Canonical Allele Identifier: CA6191006
Community Standard Title: NM_001235.5(SERPINH1):c.1059C>T (p.His353=)
Gene: SERPINH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.75571885C>T , CM000673.2:g.75571885C>T GRCh38
NC_000011.9:g.75282930C>T , CM000673.1:g.75282930C>T GRCh37
NC_000011.8:g.74960578C>T NCBI36
NG_012052.1:g.14761C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001235.5:c.1059C>T MANE Select NP_001226.2:p.His353=
ENST00000358171.8:c.1059C>T MANE Select ENSP00000350894.4:p.His353=
NM_001207014.1:c.1059C>T NP_001193943.1:p.His353=
NM_001207014.2:c.1059C>T NP_001193943.1:p.His353=
NM_001207014.3:c.1059C>T NP_001193943.1:p.His353=
NM_001235.3:c.1059C>T NP_001226.2:p.His353=
ENST00000358171.7:c.1059C>T ENSP00000350894.3:p.His353=
ENST00000524558.5:c.1059C>T ENSP00000434412.1:p.His353=
ENST00000525876.1:c.408C>T ENSP00000433532.1:p.His136=
ENST00000533449.6:c.1059C>T ENSP00000431827.2:p.His353=
ENST00000533603.5:c.1059C>T ENSP00000434657.1:p.His353=
ENST00000649490.1:c.*1710C>T ENSP00000497544.1:n.*1710C>T
XM_006718729.1:c.1059C>T XP_006718792.1:p.His353=
XM_011545326.1:c.1059C>T XP_011543628.1:p.His353=
XM_011545327.1:c.1059C>T XP_011543629.1:p.His353=
XM_024448756.1:c.1059C>T XP_024304524.1:p.His353=