Canonical Allele Identifier: CA373836402
Gene: AUH HGNC NCBI

Linked Data

gnomAD v4: 9-91361738-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91361738G>T , CM000671.2:g.91361738G>T GRCh38
NC_000009.11:g.94124020G>T , CM000671.1:g.94124020G>T GRCh37
NC_000009.10:g.93163841G>T NCBI36
NG_008017.1:g.5187C>A , LRG_449:g.5187C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375731.9:c.152C>A MANE Select ENSP00000364883.5:p.Ala51Asp
ENST00000303617.5:c.152C>A ENSP00000307334.5:p.Ala51Asp
ENST00000375731.8:c.152C>A ENSP00000364883.4:p.Ala51Asp
ENST00000478465.5:n.150C>A
NM_001306190.1:c.152C>A NP_001293119.1:p.Ala51Asp
NM_001698.2:c.152C>A , LRG_449t1:c.152C>A NP_001689.1:p.Ala51Asp
XM_005252066.2:c.152C>A XP_005252123.1:p.Ala51Asp
XM_005252067.3:c.152C>A XP_005252124.1:p.Ala51Asp
XM_005252069.3:c.152C>A XP_005252126.1:p.Ala51Asp
XM_005252072.1:c.152C>A XP_005252129.1:p.Ala51Asp
XM_006717150.2:c.152C>A XP_006717213.1:p.Ala51Asp
XM_011518800.1:c.152C>A XP_011517102.1:p.Ala51Asp
XM_011518803.1:c.152C>A XP_011517105.1:p.Ala51Asp
XM_011518804.1:c.152C>A XP_011517106.1:p.Ala51Asp
XR_929814.1:n.202C>A
NM_001351431.1:c.-246C>A NP_001338360.1:n.-246C>A
NM_001351432.1:c.-338C>A NP_001338361.1:n.-338C>A
NM_001351433.1:c.-246C>A NP_001338362.1:n.-246C>A
XM_005252066.3:c.152C>A XP_005252123.1:p.Ala51Asp
XM_005252067.4:c.152C>A XP_005252124.1:p.Ala51Asp
XM_005252069.4:c.152C>A XP_005252126.1:p.Ala51Asp
XM_005252072.2:c.152C>A XP_005252129.1:p.Ala51Asp
XM_006717150.3:c.152C>A XP_006717213.1:p.Ala51Asp
XM_011518800.3:c.152C>A XP_011517102.1:p.Ala51Asp
XM_011518803.2:c.152C>A XP_011517105.1:p.Ala51Asp
XM_017014849.1:c.152C>A XP_016870338.1:p.Ala51Asp
XR_001746328.2:n.205C>A
XR_001746329.2:n.187C>A
NM_001698.3:c.152C>A MANE Select NP_001689.1:p.Ala51Asp
NM_001306190.2:c.152C>A NP_001293119.1:p.Ala51Asp
NM_001351431.2:c.-246C>A NP_001338360.1:n.-246C>A
NM_001351432.2:c.-338C>A NP_001338361.1:n.-338C>A
NM_001351433.2:c.-246C>A NP_001338362.1:n.-246C>A