Canonical Allele Identifier: CA6191037
Community Standard Title: NM_001235.5(SERPINH1):c.1178G>A (p.Arg393Gln)
Gene: SERPINH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.75572004G>A , CM000673.2:g.75572004G>A GRCh38
NC_000011.9:g.75283049G>A , CM000673.1:g.75283049G>A GRCh37
NC_000011.8:g.74960697G>A NCBI36
NG_012052.1:g.14880G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001235.5:c.1178G>A MANE Select NP_001226.2:p.Arg393Gln
ENST00000358171.8:c.1178G>A MANE Select ENSP00000350894.4:p.Arg393Gln
NM_001207014.1:c.1178G>A NP_001193943.1:p.Arg393Gln
NM_001207014.2:c.1178G>A NP_001193943.1:p.Arg393Gln
NM_001207014.3:c.1178G>A NP_001193943.1:p.Arg393Gln
NM_001235.3:c.1178G>A NP_001226.2:p.Arg393Gln
ENST00000358171.7:c.1178G>A ENSP00000350894.3:p.Arg393Gln
ENST00000524558.5:c.1178G>A ENSP00000434412.1:p.Arg393Gln
ENST00000525876.1:c.527G>A ENSP00000433532.1:p.Arg176Gln
ENST00000526638.1:c.91G>A
ENST00000533603.5:c.1178G>A ENSP00000434657.1:p.Arg393Gln
ENST00000649490.1:c.*1829G>A ENSP00000497544.1:n.*1829G>A
XM_006718729.1:c.1178G>A XP_006718792.1:p.Arg393Gln
XM_011545326.1:c.1178G>A XP_011543628.1:p.Arg393Gln
XM_011545327.1:c.1178G>A XP_011543629.1:p.Arg393Gln
XM_024448756.1:c.1178G>A XP_024304524.1:p.Arg393Gln