Canonical Allele Identifier: CA343772853

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173907511A>G , CM000663.2:g.173907511A>G	GRCh38
NC_000001.10:g.173876649A>G , CM000663.1:g.173876649A>G	GRCh37
NC_000001.9:g.172143272A>G	NCBI36
NG_012462.1:g.14868T>C , LRG_577:g.14868T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000488.4:c.1157T>C MANE Select	NP_000479.1:p.Ile386Thr
ENST00000367698.4:c.1157T>C MANE Select	ENSP00000356671.3:p.Ile386Thr
NM_000488.3:c.1157T>C , LRG_577t1:c.1157T>C	NP_000479.1:p.Ile386Thr
NM_001365052.1:c.1013T>C	NP_001351981.1:p.Ile338Thr
NM_001365052.2:c.1013T>C	NP_001351981.1:p.Ile338Thr
NM_001386302.1:c.1280T>C	NP_001373231.1:p.Ile427Thr
NM_001386303.1:c.1238T>C	NP_001373232.1:p.Ile413Thr
NM_001386304.1:c.1136T>C	NP_001373233.1:p.Ile379Thr
NM_001386305.1:c.1100T>C	NP_001373234.1:p.Ile367Thr
NM_001386306.1:c.941T>C	NP_001373235.1:p.Ile314Thr
ENST00000367698.3:c.1157T>C	ENSP00000356671.3:p.Ile386Thr
ENST00000617423.4:c.560-18T>C	ENSP00000478688.1:n.560-18T>C
XM_005245198.2:c.1013T>C	XP_005245255.1:p.Ile338Thr