Canonical Allele Identifier: CA343773516

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878716A>G (hg19) ; chr1:g.173909578A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909578A>G , CM000663.2:g.173909578A>G	GRCh38
NC_000001.10:g.173878716A>G , CM000663.1:g.173878716A>G	GRCh37
NC_000001.9:g.172145339A>G	NCBI36
NG_012462.1:g.12801T>C , LRG_577:g.12801T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1127T>C MANE Select	ENSP00000356671.3:p.Phe376Ser
ENST00000367698.3:c.1127T>C	ENSP00000356671.3:p.Phe376Ser
ENST00000617423.4:c.560-2085T>C	ENSP00000478688.1:n.560-2085T>C
NM_000488.3:c.1127T>C , LRG_577t1:c.1127T>C	NP_000479.1:p.Phe376Ser
XM_005245198.2:c.983T>C	XP_005245255.1:p.Phe328Ser
NM_001365052.1:c.983T>C	NP_001351981.1:p.Phe328Ser
NM_000488.4:c.1127T>C MANE Select	NP_000479.1:p.Phe376Ser
NM_001365052.2:c.983T>C	NP_001351981.1:p.Phe328Ser
NM_001386302.1:c.1250T>C	NP_001373231.1:p.Phe417Ser
NM_001386303.1:c.1208T>C	NP_001373232.1:p.Phe403Ser
NM_001386304.1:c.1106T>C	NP_001373233.1:p.Phe369Ser
NM_001386305.1:c.1070T>C	NP_001373234.1:p.Phe357Ser
NM_001386306.1:c.911T>C	NP_001373235.1:p.Phe304Ser