Canonical Allele Identifier: CA343773651

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173909639-G-C
• MyVariant Identifiers: chr1:g.173878777G>C (hg19) ; chr1:g.173909639G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909639G>C , CM000663.2:g.173909639G>C	GRCh38
NC_000001.10:g.173878777G>C , CM000663.1:g.173878777G>C	GRCh37
NC_000001.9:g.172145400G>C	NCBI36
NG_012462.1:g.12740C>G , LRG_577:g.12740C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1066C>G MANE Select	ENSP00000356671.3:p.Arg356Gly
ENST00000367698.3:c.1066C>G	ENSP00000356671.3:p.Arg356Gly
ENST00000617423.4:c.560-2146C>G	ENSP00000478688.1:n.560-2146C>G
NM_000488.3:c.1066C>G , LRG_577t1:c.1066C>G	NP_000479.1:p.Arg356Gly
XM_005245198.2:c.922C>G	XP_005245255.1:p.Arg308Gly
NM_001365052.1:c.922C>G	NP_001351981.1:p.Arg308Gly
NM_000488.4:c.1066C>G MANE Select	NP_000479.1:p.Arg356Gly
NM_001365052.2:c.922C>G	NP_001351981.1:p.Arg308Gly
NM_001386302.1:c.1189C>G	NP_001373231.1:p.Arg397Gly
NM_001386303.1:c.1147C>G	NP_001373232.1:p.Arg383Gly
NM_001386304.1:c.1045C>G	NP_001373233.1:p.Arg349Gly
NM_001386305.1:c.1009C>G	NP_001373234.1:p.Arg337Gly
NM_001386306.1:c.850C>G	NP_001373235.1:p.Arg284Gly