Canonical Allele Identifier: CA343772047
Gene: SERPINC1 HGNC NCBI

Linked Data

gnomAD v4: 1-173903904-G-T
MyVariant Identifiers: chr1:g.173873042G>T (hg19) chr1:g.173903904G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903904G>T , CM000663.2:g.173903904G>T GRCh38
NC_000001.10:g.173873042G>T , CM000663.1:g.173873042G>T GRCh37
NC_000001.9:g.172139665G>T NCBI36
NG_012462.1:g.18475C>A , LRG_577:g.18475C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1380C>A MANE Select ENSP00000356671.3:p.Asn460Lys
ENST00000367698.3:c.1380C>A ENSP00000356671.3:p.Asn460Lys
ENST00000617423.4:c.765C>A ENSP00000478688.1:p.Asn255Lys
NM_000488.3:c.1380C>A , LRG_577t1:c.1380C>A NP_000479.1:p.Asn460Lys
XM_005245198.2:c.1236C>A XP_005245255.1:p.Asn412Lys
NM_001365052.1:c.1236C>A NP_001351981.1:p.Asn412Lys
NM_000488.4:c.1380C>A MANE Select NP_000479.1:p.Asn460Lys
NM_001365052.2:c.1236C>A NP_001351981.1:p.Asn412Lys
NM_001386302.1:c.1503C>A NP_001373231.1:p.Asn501Lys
NM_001386303.1:c.1461C>A NP_001373232.1:p.Asn487Lys
NM_001386304.1:c.1359C>A NP_001373233.1:p.Asn453Lys
NM_001386305.1:c.1323C>A NP_001373234.1:p.Asn441Lys
NM_001386306.1:c.1164C>A NP_001373235.1:p.Asn388Lys
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