Canonical Allele Identifier: CA2615177305

Gene: SERPINH1

Linked Data

• gnomAD v4: 11-75568887-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75568888del , CM000673.2:g.75568888del	GRCh38
NC_000011.9:g.75279933del , CM000673.1:g.75279933del	GRCh37
NC_000011.8:g.74957581del	NCBI36
NG_012052.1:g.11764del

Transcript Alleles

HGVS	Amino-acid change
ENST00000358171.8:c.722-51del MANE Select	ENSP00000350894.4:n.722-51del
ENST00000533449.6:c.722-51del	ENSP00000431827.2:n.722-51del
ENST00000649490.1:c.722-51del	ENSP00000497544.1:n.722-51del
ENST00000358171.7:c.722-51del	ENSP00000350894.3:n.722-51del
ENST00000524558.5:c.722-51del	ENSP00000434412.1:n.722-51del
ENST00000525611.5:c.722-51del	ENSP00000435452.1:n.722-51del
ENST00000525876.1:c.71-51del	ENSP00000433532.1:n.71-51del
ENST00000526397.5:c.722-51del	ENSP00000434964.1:n.722-51del
ENST00000530284.5:c.722-51del	ENSP00000436305.1:n.722-51del
ENST00000532356.5:c.722-51del	ENSP00000436040.1:n.722-51del
ENST00000533603.5:c.722-51del	ENSP00000434657.1:n.722-51del
NM_001207014.1:c.722-51del	NP_001193943.1:n.722-51del
NM_001235.3:c.722-51del	NP_001226.2:n.722-51del
XM_006718729.1:c.722-51del	XP_006718792.1:n.722-51del
XM_011545326.1:c.722-51del	XP_011543628.1:n.722-51del
XM_011545327.1:c.722-51del	XP_011543629.1:n.722-51del
XM_024448756.1:c.722-51del	XP_024304524.1:n.722-51del
NM_001207014.2:c.722-51del	NP_001193943.1:n.722-51del
NM_001235.5:c.722-51del MANE Select	NP_001226.2:n.722-51del
NM_001207014.3:c.722-51del	NP_001193943.1:n.722-51del