Canonical Allele Identifier: CA195931368
Gene: AUH HGNC NCBI

Linked Data

dbSNP Id: rs908561470
gnomAD v4: 9-91361817-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91361817C>T , CM000671.2:g.91361817C>T GRCh38
NC_000009.11:g.94124099C>T , CM000671.1:g.94124099C>T GRCh37
NC_000009.10:g.93163920C>T NCBI36
NG_008017.1:g.5108G>A , LRG_449:g.5108G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375731.9:c.73G>A MANE Select ENSP00000364883.5:p.Ala25Thr
ENST00000303617.5:c.73G>A ENSP00000307334.5:p.Ala25Thr
ENST00000375731.8:c.73G>A ENSP00000364883.4:p.Ala25Thr
ENST00000478465.5:n.71G>A
NM_001306190.1:c.73G>A NP_001293119.1:p.Ala25Thr
NM_001698.2:c.73G>A , LRG_449t1:c.73G>A NP_001689.1:p.Ala25Thr
XM_005252066.2:c.73G>A XP_005252123.1:p.Ala25Thr
XM_005252067.3:c.73G>A XP_005252124.1:p.Ala25Thr
XM_005252069.3:c.73G>A XP_005252126.1:p.Ala25Thr
XM_005252072.1:c.73G>A XP_005252129.1:p.Ala25Thr
XM_006717150.2:c.73G>A XP_006717213.1:p.Ala25Thr
XM_011518800.1:c.73G>A XP_011517102.1:p.Ala25Thr
XM_011518803.1:c.73G>A XP_011517105.1:p.Ala25Thr
XM_011518804.1:c.73G>A XP_011517106.1:p.Ala25Thr
XR_929814.1:n.123G>A
NM_001351431.1:c.-325G>A NP_001338360.1:n.-325G>A
NM_001351432.1:c.-417G>A NP_001338361.1:n.-417G>A
NM_001351433.1:c.-325G>A NP_001338362.1:n.-325G>A
XM_005252066.3:c.73G>A XP_005252123.1:p.Ala25Thr
XM_005252067.4:c.73G>A XP_005252124.1:p.Ala25Thr
XM_005252069.4:c.73G>A XP_005252126.1:p.Ala25Thr
XM_005252072.2:c.73G>A XP_005252129.1:p.Ala25Thr
XM_006717150.3:c.73G>A XP_006717213.1:p.Ala25Thr
XM_011518800.3:c.73G>A XP_011517102.1:p.Ala25Thr
XM_011518803.2:c.73G>A XP_011517105.1:p.Ala25Thr
XM_017014849.1:c.73G>A XP_016870338.1:p.Ala25Thr
XR_001746328.2:n.126G>A
XR_001746329.2:n.108G>A
NM_001698.3:c.73G>A MANE Select NP_001689.1:p.Ala25Thr
NM_001306190.2:c.73G>A NP_001293119.1:p.Ala25Thr
NM_001351431.2:c.-325G>A NP_001338360.1:n.-325G>A
NM_001351432.2:c.-417G>A NP_001338361.1:n.-417G>A
NM_001351433.2:c.-325G>A NP_001338362.1:n.-325G>A