Canonical Allele Identifier: CA343773519

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173909579-A-G
• MyVariant Identifiers: chr1:g.173878717A>G (hg19) ; chr1:g.173909579A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909579A>G , CM000663.2:g.173909579A>G	GRCh38
NC_000001.10:g.173878717A>G , CM000663.1:g.173878717A>G	GRCh37
NC_000001.9:g.172145340A>G	NCBI36
NG_012462.1:g.12800T>C , LRG_577:g.12800T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1126T>C MANE Select	ENSP00000356671.3:p.Phe376Leu
ENST00000367698.3:c.1126T>C	ENSP00000356671.3:p.Phe376Leu
ENST00000617423.4:c.560-2086T>C	ENSP00000478688.1:n.560-2086T>C
NM_000488.3:c.1126T>C , LRG_577t1:c.1126T>C	NP_000479.1:p.Phe376Leu
XM_005245198.2:c.982T>C	XP_005245255.1:p.Phe328Leu
NM_001365052.1:c.982T>C	NP_001351981.1:p.Phe328Leu
NM_000488.4:c.1126T>C MANE Select	NP_000479.1:p.Phe376Leu
NM_001365052.2:c.982T>C	NP_001351981.1:p.Phe328Leu
NM_001386302.1:c.1249T>C	NP_001373231.1:p.Phe417Leu
NM_001386303.1:c.1207T>C	NP_001373232.1:p.Phe403Leu
NM_001386304.1:c.1105T>C	NP_001373233.1:p.Phe369Leu
NM_001386305.1:c.1069T>C	NP_001373234.1:p.Phe357Leu
NM_001386306.1:c.910T>C	NP_001373235.1:p.Phe304Leu