Canonical Allele Identifier: CA1863689092

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220968G= , CM000671.2:g.91220968G=	GRCh38
NC_000009.11:g.93983250G= , CM000671.1:g.93983250G=	GRCh37
NC_000009.10:g.93023071G=	NCBI36
NG_008017.1:g.145957C= , LRG_449:g.145957C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.680C= MANE Select	ENSP00000364883.5:p.Ala227=
ENST00000303617.5:c.593C=	ENSP00000307334.5:p.Ala198=
ENST00000375731.8:c.680C=	ENSP00000364883.4:p.Ala227=
NM_001306190.1:c.593C=	NP_001293119.1:p.Ala198=
NM_001698.2:c.680C= , LRG_449t1:c.680C=	NP_001689.1:p.Ala227=
XM_005252066.2:c.710C=	XP_005252123.1:p.Ala237=
XM_005252067.3:c.710C=	XP_005252124.1:p.Ala237=
XM_005252069.3:c.710C=	XP_005252126.1:p.Ala237=
XM_005252073.2:c.218C=	XP_005252130.1:p.Ala73=
XM_006717150.2:c.623C=	XP_006717213.1:p.Ala208=
XM_011518801.1:c.356C=	XP_011517103.1:p.Ala119=
XM_011518802.1:c.353C=	XP_011517104.1:p.Ala118=
NM_001351431.1:c.353C=	NP_001338360.1:p.Ala118=
NM_001351432.1:c.353C=	NP_001338361.1:p.Ala118=
NM_001351433.1:c.353C=	NP_001338362.1:p.Ala118=
XM_005252066.3:c.710C=	XP_005252123.1:p.Ala237=
XM_005252067.4:c.710C=	XP_005252124.1:p.Ala237=
XM_005252069.4:c.710C=	XP_005252126.1:p.Ala237=
XM_006717150.3:c.623C=	XP_006717213.1:p.Ala208=
XM_017014849.1:c.680C=	XP_016870338.1:p.Ala227=
XR_001746328.2:n.905C=
XR_001746329.2:n.857C=
NM_001698.3:c.680C= MANE Select	NP_001689.1:p.Ala227=
NM_001306190.2:c.593C=	NP_001293119.1:p.Ala198=
NM_001351431.2:c.353C=	NP_001338360.1:p.Ala118=
NM_001351432.2:c.353C=	NP_001338361.1:p.Ala118=
NM_001351433.2:c.353C=	NP_001338362.1:p.Ala118=