Canonical Allele Identifier: CA10631544

Gene: SERPINH1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75572608C>A , CM000673.2:g.75572608C>A	GRCh38
NC_000011.9:g.75283653C>A , CM000673.1:g.75283653C>A	GRCh37
NC_000011.8:g.74961301C>A	NCBI36
NG_012052.1:g.15484C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358171.8:c.*525C>A MANE Select	ENSP00000350894.4:n.*525C>A
ENST00000358171.7:c.*525C>A	ENSP00000350894.3:n.*525C>A
ENST00000524558.5:c.*525C>A	ENSP00000434412.1:n.*525C>A
ENST00000525876.1:c.*525C>A	ENSP00000433532.1:n.*525C>A
ENST00000526638.1:c.544C>A
ENST00000533603.5:c.*525C>A	ENSP00000434657.1:n.*525C>A
NM_001207014.1:c.*525C>A	NP_001193943.1:n.*525C>A
NM_001235.3:c.*525C>A	NP_001226.2:n.*525C>A
XM_006718729.1:c.*525C>A	XP_006718792.1:n.*525C>A
XM_011545326.1:c.*525C>A	XP_011543628.1:n.*525C>A
XM_011545327.1:c.*525C>A	XP_011543629.1:n.*525C>A
XM_024448756.1:c.*525C>A	XP_024304524.1:n.*525C>A
NM_001207014.2:c.*525C>A	NP_001193943.1:n.*525C>A
NM_001235.5:c.*525C>A MANE Select	NP_001226.2:n.*525C>A
NM_001207014.3:c.*525C>A	NP_001193943.1:n.*525C>A