Canonical Allele Identifier: CA1863721480
Gene: AUH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91297996T= , CM000671.2:g.91297996T= GRCh38
NC_000009.11:g.94060278T= , CM000671.1:g.94060278T= GRCh37
NC_000009.10:g.93100099T= NCBI36
NG_008017.1:g.68929A= , LRG_449:g.68929A=

Transcript Alleles

HGVS Amino-acid change
ENST00000375731.9:c.586A= MANE Select ENSP00000364883.5:p.Ile196=
ENST00000303617.5:c.499A= ENSP00000307334.5:p.Ile167=
ENST00000375731.8:c.586A= ENSP00000364883.4:p.Ile196=
ENST00000478465.5:n.746A=
NM_001306190.1:c.499A= NP_001293119.1:p.Ile167=
NM_001698.2:c.586A= , LRG_449t1:c.586A= NP_001689.1:p.Ile196=
XM_005252066.2:c.616A= XP_005252123.1:p.Ile206=
XM_005252067.3:c.616A= XP_005252124.1:p.Ile206=
XM_005252069.3:c.616A= XP_005252126.1:p.Ile206=
XM_005252072.1:c.586A= XP_005252129.1:p.Ile196=
XM_005252073.2:c.124A= XP_005252130.1:p.Ile42=
XM_006717150.2:c.529A= XP_006717213.1:p.Ile177=
XM_011518800.1:c.616A= XP_011517102.1:p.Ile206=
XM_011518801.1:c.262A= XP_011517103.1:p.Ile88=
XM_011518802.1:c.259A= XP_011517104.1:p.Ile87=
NM_001351431.1:c.259A= NP_001338360.1:p.Ile87=
NM_001351432.1:c.259A= NP_001338361.1:p.Ile87=
NM_001351433.1:c.259A= NP_001338362.1:p.Ile87=
XM_005252066.3:c.616A= XP_005252123.1:p.Ile206=
XM_005252067.4:c.616A= XP_005252124.1:p.Ile206=
XM_005252069.4:c.616A= XP_005252126.1:p.Ile206=
XM_005252072.2:c.586A= XP_005252129.1:p.Ile196=
XM_006717150.3:c.529A= XP_006717213.1:p.Ile177=
XM_011518800.3:c.616A= XP_011517102.1:p.Ile206=
XM_017014849.1:c.586A= XP_016870338.1:p.Ile196=
XR_001746328.2:n.669A=
XR_001746329.2:n.621A=
NM_001698.3:c.586A= MANE Select NP_001689.1:p.Ile196=
NM_001306190.2:c.499A= NP_001293119.1:p.Ile167=
NM_001351431.2:c.259A= NP_001338360.1:p.Ile87=
NM_001351432.2:c.259A= NP_001338361.1:p.Ile87=
NM_001351433.2:c.259A= NP_001338362.1:p.Ile87=