Canonical Allele Identifier: CA343773664

Gene: SERPINC1

Linked Data

• ClinVar Variation Id: 2734039
• ClinVar RCV Id: RCV003527186
• MyVariant Identifiers: chr1:g.173878785G>A (hg19) ; chr1:g.173909647G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909647G>A , CM000663.2:g.173909647G>A	GRCh38
NC_000001.10:g.173878785G>A , CM000663.1:g.173878785G>A	GRCh37
NC_000001.9:g.172145408G>A	NCBI36
NG_012462.1:g.12732C>T , LRG_577:g.12732C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1058C>T MANE Select	ENSP00000356671.3:p.Pro353Leu
ENST00000367698.3:c.1058C>T	ENSP00000356671.3:p.Pro353Leu
ENST00000617423.4:c.560-2154C>T	ENSP00000478688.1:n.560-2154C>T
NM_000488.3:c.1058C>T , LRG_577t1:c.1058C>T	NP_000479.1:p.Pro353Leu
XM_005245198.2:c.914C>T	XP_005245255.1:p.Pro305Leu
NM_001365052.1:c.914C>T	NP_001351981.1:p.Pro305Leu
NM_000488.4:c.1058C>T MANE Select	NP_000479.1:p.Pro353Leu
NM_001365052.2:c.914C>T	NP_001351981.1:p.Pro305Leu
NM_001386302.1:c.1181C>T	NP_001373231.1:p.Pro394Leu
NM_001386303.1:c.1139C>T	NP_001373232.1:p.Pro380Leu
NM_001386304.1:c.1037C>T	NP_001373233.1:p.Pro346Leu
NM_001386305.1:c.1001C>T	NP_001373234.1:p.Pro334Leu
NM_001386306.1:c.842C>T	NP_001373235.1:p.Pro281Leu