Canonical Allele Identifier: CA343772535
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873137G>C (hg19) chr1:g.173903999G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903999G>C , CM000663.2:g.173903999G>C GRCh38
NC_000001.10:g.173873137G>C , CM000663.1:g.173873137G>C GRCh37
NC_000001.9:g.172139760G>C NCBI36
NG_012462.1:g.18380C>G , LRG_577:g.18380C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1285C>G MANE Select ENSP00000356671.3:p.Pro429Ala
ENST00000367698.3:c.1285C>G ENSP00000356671.3:p.Pro429Ala
ENST00000617423.4:c.670C>G ENSP00000478688.1:p.Pro224Ala
NM_000488.3:c.1285C>G , LRG_577t1:c.1285C>G NP_000479.1:p.Pro429Ala
XM_005245198.2:c.1141C>G XP_005245255.1:p.Pro381Ala
NM_001365052.1:c.1141C>G NP_001351981.1:p.Pro381Ala
NM_000488.4:c.1285C>G MANE Select NP_000479.1:p.Pro429Ala
NM_001365052.2:c.1141C>G NP_001351981.1:p.Pro381Ala
NM_001386302.1:c.1408C>G NP_001373231.1:p.Pro470Ala
NM_001386303.1:c.1366C>G NP_001373232.1:p.Pro456Ala
NM_001386304.1:c.1264C>G NP_001373233.1:p.Pro422Ala
NM_001386305.1:c.1228C>G NP_001373234.1:p.Pro410Ala
NM_001386306.1:c.1069C>G NP_001373235.1:p.Pro357Ala
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