Canonical Allele Identifier: CA1983388727
Gene: SERPINH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.75568878T= , CM000673.2:g.75568878T= GRCh38
NC_000011.9:g.75279923T= , CM000673.1:g.75279923T= GRCh37
NC_000011.8:g.74957571T= NCBI36
NG_012052.1:g.11754T=

Transcript Alleles

HGVS Amino-acid change
ENST00000358171.8:c.721+49T= MANE Select ENSP00000350894.4:n.721+49T=
ENST00000533449.6:c.721+49T= ENSP00000431827.2:n.721+49T=
ENST00000649490.1:c.721+49T= ENSP00000497544.1:n.721+49T=
ENST00000358171.7:c.721+49T= ENSP00000350894.3:n.721+49T=
ENST00000524558.5:c.721+49T= ENSP00000434412.1:n.721+49T=
ENST00000525611.5:c.721+49T= ENSP00000435452.1:n.721+49T=
ENST00000525876.1:c.70+49T= ENSP00000433532.1:n.70+49T=
ENST00000526397.5:c.721+49T= ENSP00000434964.1:n.721+49T=
ENST00000530284.5:c.721+49T= ENSP00000436305.1:n.721+49T=
ENST00000532356.5:c.721+49T= ENSP00000436040.1:n.721+49T=
ENST00000533603.5:c.721+49T= ENSP00000434657.1:n.721+49T=
NM_001207014.1:c.721+49T= NP_001193943.1:n.721+49T=
NM_001235.3:c.721+49T= NP_001226.2:n.721+49T=
XM_006718729.1:c.721+49T= XP_006718792.1:n.721+49T=
XM_011545326.1:c.721+49T= XP_011543628.1:n.721+49T=
XM_011545327.1:c.721+49T= XP_011543629.1:n.721+49T=
XM_024448756.1:c.721+49T= XP_024304524.1:n.721+49T=
NM_001207014.2:c.721+49T= NP_001193943.1:n.721+49T=
NM_001235.5:c.721+49T= MANE Select NP_001226.2:n.721+49T=
NM_001207014.3:c.721+49T= NP_001193943.1:n.721+49T=