Canonical Allele Identifier: CA10635675
Community Standard Title: NM_001235.5(SERPINH1):c.*354G>T
Gene: SERPINH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.75572437G>T , CM000673.2:g.75572437G>T GRCh38
NC_000011.9:g.75283482G>T , CM000673.1:g.75283482G>T GRCh37
NC_000011.8:g.74961130G>T NCBI36
NG_012052.1:g.15313G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001235.5:c.*354G>T MANE Select NP_001226.2:n.*354G>T
ENST00000358171.8:c.*354G>T MANE Select ENSP00000350894.4:n.*354G>T
NM_001207014.1:c.*354G>T NP_001193943.1:n.*354G>T
NM_001207014.2:c.*354G>T NP_001193943.1:n.*354G>T
NM_001207014.3:c.*354G>T NP_001193943.1:n.*354G>T
NM_001235.3:c.*354G>T NP_001226.2:n.*354G>T
ENST00000358171.7:c.*354G>T ENSP00000350894.3:n.*354G>T
ENST00000524558.5:c.*354G>T ENSP00000434412.1:n.*354G>T
ENST00000525876.1:c.*354G>T ENSP00000433532.1:n.*354G>T
ENST00000526638.1:c.486+38G>T
ENST00000533603.5:c.*354G>T ENSP00000434657.1:n.*354G>T
ENST00000649490.1:c.*2262G>T ENSP00000497544.1:n.*2262G>T
XM_006718729.1:c.*354G>T XP_006718792.1:n.*354G>T
XM_011545326.1:c.*354G>T XP_011543628.1:n.*354G>T
XM_011545327.1:c.*354G>T XP_011543629.1:n.*354G>T
XM_024448756.1:c.*354G>T XP_024304524.1:n.*354G>T