Canonical Allele Identifier: CA343772040

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873041G>C (hg19) ; chr1:g.173903903G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903903G>C , CM000663.2:g.173903903G>C	GRCh38
NC_000001.10:g.173873041G>C , CM000663.1:g.173873041G>C	GRCh37
NC_000001.9:g.172139664G>C	NCBI36
NG_012462.1:g.18476C>G , LRG_577:g.18476C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1381C>G MANE Select	ENSP00000356671.3:p.Pro461Ala
ENST00000367698.3:c.1381C>G	ENSP00000356671.3:p.Pro461Ala
ENST00000617423.4:c.766C>G	ENSP00000478688.1:p.Pro256Ala
NM_000488.3:c.1381C>G , LRG_577t1:c.1381C>G	NP_000479.1:p.Pro461Ala
XM_005245198.2:c.1237C>G	XP_005245255.1:p.Pro413Ala
NM_001365052.1:c.1237C>G	NP_001351981.1:p.Pro413Ala
NM_000488.4:c.1381C>G MANE Select	NP_000479.1:p.Pro461Ala
NM_001365052.2:c.1237C>G	NP_001351981.1:p.Pro413Ala
NM_001386302.1:c.1504C>G	NP_001373231.1:p.Pro502Ala
NM_001386303.1:c.1462C>G	NP_001373232.1:p.Pro488Ala
NM_001386304.1:c.1360C>G	NP_001373233.1:p.Pro454Ala
NM_001386305.1:c.1324C>G	NP_001373234.1:p.Pro442Ala
NM_001386306.1:c.1165C>G	NP_001373235.1:p.Pro389Ala