Canonical Allele Identifier: CA1863736708
Gene: AUH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91361762C= , CM000671.2:g.91361762C= GRCh38
NC_000009.11:g.94124044C= , CM000671.1:g.94124044C= GRCh37
NC_000009.10:g.93163865C= NCBI36
NG_008017.1:g.5163G= , LRG_449:g.5163G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375731.9:c.128G= MANE Select ENSP00000364883.5:p.Arg43=
ENST00000303617.5:c.128G= ENSP00000307334.5:p.Arg43=
ENST00000375731.8:c.128G= ENSP00000364883.4:p.Arg43=
ENST00000478465.5:n.126G=
NM_001306190.1:c.128G= NP_001293119.1:p.Arg43=
NM_001698.2:c.128G= , LRG_449t1:c.128G= NP_001689.1:p.Arg43=
XM_005252066.2:c.128G= XP_005252123.1:p.Arg43=
XM_005252067.3:c.128G= XP_005252124.1:p.Arg43=
XM_005252069.3:c.128G= XP_005252126.1:p.Arg43=
XM_005252072.1:c.128G= XP_005252129.1:p.Arg43=
XM_006717150.2:c.128G= XP_006717213.1:p.Arg43=
XM_011518800.1:c.128G= XP_011517102.1:p.Arg43=
XM_011518803.1:c.128G= XP_011517105.1:p.Arg43=
XM_011518804.1:c.128G= XP_011517106.1:p.Arg43=
XR_929814.1:n.178G=
NM_001351431.1:c.-270G= NP_001338360.1:n.-270G=
NM_001351432.1:c.-362G= NP_001338361.1:n.-362G=
NM_001351433.1:c.-270G= NP_001338362.1:n.-270G=
XM_005252066.3:c.128G= XP_005252123.1:p.Arg43=
XM_005252067.4:c.128G= XP_005252124.1:p.Arg43=
XM_005252069.4:c.128G= XP_005252126.1:p.Arg43=
XM_005252072.2:c.128G= XP_005252129.1:p.Arg43=
XM_006717150.3:c.128G= XP_006717213.1:p.Arg43=
XM_011518800.3:c.128G= XP_011517102.1:p.Arg43=
XM_011518803.2:c.128G= XP_011517105.1:p.Arg43=
XM_017014849.1:c.128G= XP_016870338.1:p.Arg43=
XR_001746328.2:n.181G=
XR_001746329.2:n.163G=
NM_001698.3:c.128G= MANE Select NP_001689.1:p.Arg43=
NM_001306190.2:c.128G= NP_001293119.1:p.Arg43=
NM_001351431.2:c.-270G= NP_001338360.1:n.-270G=
NM_001351432.2:c.-362G= NP_001338361.1:n.-362G=
NM_001351433.2:c.-270G= NP_001338362.1:n.-270G=