Canonical Allele Identifier: CA343772058
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873044T>C (hg19) chr1:g.173903906T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903906T>C , CM000663.2:g.173903906T>C GRCh38
NC_000001.10:g.173873044T>C , CM000663.1:g.173873044T>C GRCh37
NC_000001.9:g.172139667T>C NCBI36
NG_012462.1:g.18473A>G , LRG_577:g.18473A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1378A>G MANE Select ENSP00000356671.3:p.Asn460Asp
ENST00000367698.3:c.1378A>G ENSP00000356671.3:p.Asn460Asp
ENST00000617423.4:c.763A>G ENSP00000478688.1:p.Asn255Asp
NM_000488.3:c.1378A>G , LRG_577t1:c.1378A>G NP_000479.1:p.Asn460Asp
XM_005245198.2:c.1234A>G XP_005245255.1:p.Asn412Asp
NM_001365052.1:c.1234A>G NP_001351981.1:p.Asn412Asp
NM_000488.4:c.1378A>G MANE Select NP_000479.1:p.Asn460Asp
NM_001365052.2:c.1234A>G NP_001351981.1:p.Asn412Asp
NM_001386302.1:c.1501A>G NP_001373231.1:p.Asn501Asp
NM_001386303.1:c.1459A>G NP_001373232.1:p.Asn487Asp
NM_001386304.1:c.1357A>G NP_001373233.1:p.Asn453Asp
NM_001386305.1:c.1321A>G NP_001373234.1:p.Asn441Asp
NM_001386306.1:c.1162A>G NP_001373235.1:p.Asn388Asp
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