Canonical Allele Identifier: CA1863689145

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220989C= , CM000671.2:g.91220989C=	GRCh38
NC_000009.11:g.93983271C= , CM000671.1:g.93983271C=	GRCh37
NC_000009.10:g.93023092C=	NCBI36
NG_008017.1:g.145936G= , LRG_449:g.145936G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.659G= MANE Select	ENSP00000364883.5:p.Gly220=
ENST00000303617.5:c.572G=	ENSP00000307334.5:p.Gly191=
ENST00000375731.8:c.659G=	ENSP00000364883.4:p.Gly220=
NM_001306190.1:c.572G=	NP_001293119.1:p.Gly191=
NM_001698.2:c.659G= , LRG_449t1:c.659G=	NP_001689.1:p.Gly220=
XM_005252066.2:c.689G=	XP_005252123.1:p.Gly230=
XM_005252067.3:c.689G=	XP_005252124.1:p.Gly230=
XM_005252069.3:c.689G=	XP_005252126.1:p.Gly230=
XM_005252073.2:c.197G=	XP_005252130.1:p.Gly66=
XM_006717150.2:c.602G=	XP_006717213.1:p.Gly201=
XM_011518801.1:c.335G=	XP_011517103.1:p.Gly112=
XM_011518802.1:c.332G=	XP_011517104.1:p.Gly111=
NM_001351431.1:c.332G=	NP_001338360.1:p.Gly111=
NM_001351432.1:c.332G=	NP_001338361.1:p.Gly111=
NM_001351433.1:c.332G=	NP_001338362.1:p.Gly111=
XM_005252066.3:c.689G=	XP_005252123.1:p.Gly230=
XM_005252067.4:c.689G=	XP_005252124.1:p.Gly230=
XM_005252069.4:c.689G=	XP_005252126.1:p.Gly230=
XM_006717150.3:c.602G=	XP_006717213.1:p.Gly201=
XM_017014849.1:c.659G=	XP_016870338.1:p.Gly220=
XR_001746328.2:n.884G=
XR_001746329.2:n.836G=
NM_001698.3:c.659G= MANE Select	NP_001689.1:p.Gly220=
NM_001306190.2:c.572G=	NP_001293119.1:p.Gly191=
NM_001351431.2:c.332G=	NP_001338360.1:p.Gly111=
NM_001351432.2:c.332G=	NP_001338361.1:p.Gly111=
NM_001351433.2:c.332G=	NP_001338362.1:p.Gly111=