Canonical Allele Identifier: CA343776778

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911971A>T , CM000663.2:g.173911971A>T	GRCh38
NC_000001.10:g.173881109A>T , CM000663.1:g.173881109A>T	GRCh37
NC_000001.9:g.172147732A>T	NCBI36
NG_012462.1:g.10408T>A , LRG_577:g.10408T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000488.4:c.452T>A MANE Select	NP_000479.1:p.Ile151Asn
ENST00000367698.4:c.452T>A MANE Select	ENSP00000356671.3:p.Ile151Asn
NM_000488.3:c.452T>A , LRG_577t1:c.452T>A	NP_000479.1:p.Ile151Asn
NM_001365052.1:c.308T>A	NP_001351981.1:p.Ile103Asn
NM_001365052.2:c.308T>A	NP_001351981.1:p.Ile103Asn
NM_001386302.1:c.452T>A	NP_001373231.1:p.Ile151Asn
NM_001386303.1:c.533T>A	NP_001373232.1:p.Ile178Asn
NM_001386304.1:c.452T>A	NP_001373233.1:p.Ile151Asn
NM_001386305.1:c.452T>A	NP_001373234.1:p.Ile151Asn
NM_001386306.1:c.409-1080T>A	NP_001373235.1:n.409-1080T>A
ENST00000367698.3:c.452T>A	ENSP00000356671.3:p.Ile151Asn
ENST00000487183.1:n.157T>A
ENST00000617423.4:c.452T>A	ENSP00000478688.1:p.Ile151Asn
XM_005245198.2:c.308T>A	XP_005245255.1:p.Ile103Asn