Canonical Allele Identifier: CA10588848

Gene: SERPINH1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75568818T>C , CM000673.2:g.75568818T>C	GRCh38
NC_000011.9:g.75279863T>C , CM000673.1:g.75279863T>C	GRCh37
NC_000011.8:g.74957511T>C	NCBI36
NG_012052.1:g.11694T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358171.8:c.710T>C MANE Select	ENSP00000350894.4:p.Met237Thr
ENST00000533449.6:c.710T>C	ENSP00000431827.2:p.Met237Thr
ENST00000649490.1:c.710T>C	ENSP00000497544.1:p.Met237Thr
ENST00000358171.7:c.710T>C	ENSP00000350894.3:p.Met237Thr
ENST00000524558.5:c.710T>C	ENSP00000434412.1:p.Met237Thr
ENST00000525611.5:c.710T>C	ENSP00000435452.1:p.Met237Thr
ENST00000525876.1:c.59T>C	ENSP00000433532.1:p.Met20Thr
ENST00000526397.5:c.710T>C	ENSP00000434964.1:p.Met237Thr
ENST00000530284.5:c.710T>C	ENSP00000436305.1:p.Met237Thr
ENST00000532356.5:c.710T>C	ENSP00000436040.1:p.Met237Thr
ENST00000533603.5:c.710T>C	ENSP00000434657.1:p.Met237Thr
NM_001207014.1:c.710T>C	NP_001193943.1:p.Met237Thr
NM_001235.3:c.710T>C	NP_001226.2:p.Met237Thr
XM_006718729.1:c.710T>C	XP_006718792.1:p.Met237Thr
XM_011545326.1:c.710T>C	XP_011543628.1:p.Met237Thr
XM_011545327.1:c.710T>C	XP_011543629.1:p.Met237Thr
XM_024448756.1:c.710T>C	XP_024304524.1:p.Met237Thr
NM_001207014.2:c.710T>C	NP_001193943.1:p.Met237Thr
NM_001235.5:c.710T>C MANE Select	NP_001226.2:p.Met237Thr
NM_001207014.3:c.710T>C	NP_001193943.1:p.Met237Thr