Canonical Allele Identifier: CA343773674

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173909650-A-G
• MyVariant Identifiers: chr1:g.173878788A>G (hg19) ; chr1:g.173909650A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909650A>G , CM000663.2:g.173909650A>G	GRCh38
NC_000001.10:g.173878788A>G , CM000663.1:g.173878788A>G	GRCh37
NC_000001.9:g.172145411A>G	NCBI36
NG_012462.1:g.12729T>C , LRG_577:g.12729T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1055T>C MANE Select	ENSP00000356671.3:p.Met352Thr
ENST00000367698.3:c.1055T>C	ENSP00000356671.3:p.Met352Thr
ENST00000617423.4:c.560-2157T>C	ENSP00000478688.1:n.560-2157T>C
NM_000488.3:c.1055T>C , LRG_577t1:c.1055T>C	NP_000479.1:p.Met352Thr
XM_005245198.2:c.911T>C	XP_005245255.1:p.Met304Thr
NM_001365052.1:c.911T>C	NP_001351981.1:p.Met304Thr
NM_000488.4:c.1055T>C MANE Select	NP_000479.1:p.Met352Thr
NM_001365052.2:c.911T>C	NP_001351981.1:p.Met304Thr
NM_001386302.1:c.1178T>C	NP_001373231.1:p.Met393Thr
NM_001386303.1:c.1136T>C	NP_001373232.1:p.Met379Thr
NM_001386304.1:c.1034T>C	NP_001373233.1:p.Met345Thr
NM_001386305.1:c.998T>C	NP_001373234.1:p.Met333Thr
NM_001386306.1:c.839T>C	NP_001373235.1:p.Met280Thr