Canonical Allele Identifier: CA1863688899

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220835G= , CM000671.2:g.91220835G=	GRCh38
NC_000009.11:g.93983117G= , CM000671.1:g.93983117G=	GRCh37
NC_000009.10:g.93022938G=	NCBI36
NG_008017.1:g.146090C= , LRG_449:g.146090C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.813C= MANE Select	ENSP00000364883.5:p.Ala271=
ENST00000303617.5:c.726C=	ENSP00000307334.5:p.Ala242=
ENST00000375731.8:c.813C=	ENSP00000364883.4:p.Ala271=
ENST00000473695.1:n.85C=
NM_001306190.1:c.726C=	NP_001293119.1:p.Ala242=
NM_001698.2:c.813C= , LRG_449t1:c.813C=	NP_001689.1:p.Ala271=
XM_005252066.2:c.843C=	XP_005252123.1:p.Ala281=
XM_005252067.3:c.843C=	XP_005252124.1:p.Ala281=
XM_005252069.3:c.843C=	XP_005252126.1:p.Ala281=
XM_005252073.2:c.351C=	XP_005252130.1:p.Ala117=
XM_006717150.2:c.756C=	XP_006717213.1:p.Ala252=
XM_011518801.1:c.489C=	XP_011517103.1:p.Ala163=
XM_011518802.1:c.486C=	XP_011517104.1:p.Ala162=
NM_001351431.1:c.486C=	NP_001338360.1:p.Ala162=
NM_001351432.1:c.486C=	NP_001338361.1:p.Ala162=
NM_001351433.1:c.486C=	NP_001338362.1:p.Ala162=
XM_005252066.3:c.843C=	XP_005252123.1:p.Ala281=
XM_005252067.4:c.843C=	XP_005252124.1:p.Ala281=
XM_005252069.4:c.843C=	XP_005252126.1:p.Ala281=
XM_006717150.3:c.756C=	XP_006717213.1:p.Ala252=
XM_017014849.1:c.813C=	XP_016870338.1:p.Ala271=
XR_001746328.2:n.1038C=
XR_001746329.2:n.990C=
NM_001698.3:c.813C= MANE Select	NP_001689.1:p.Ala271=
NM_001306190.2:c.726C=	NP_001293119.1:p.Ala242=
NM_001351431.2:c.486C=	NP_001338360.1:p.Ala162=
NM_001351432.2:c.486C=	NP_001338361.1:p.Ala162=
NM_001351433.2:c.486C=	NP_001338362.1:p.Ala162=