Canonical Allele Identifier: CA1863688883

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220821C= , CM000671.2:g.91220821C=	GRCh38
NC_000009.11:g.93983103C= , CM000671.1:g.93983103C=	GRCh37
NC_000009.10:g.93022924C=	NCBI36
NG_008017.1:g.146104G= , LRG_449:g.146104G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.827G= MANE Select	ENSP00000364883.5:p.Arg276=
ENST00000303617.5:c.740G=	ENSP00000307334.5:p.Arg247=
ENST00000375731.8:c.827G=	ENSP00000364883.4:p.Arg276=
ENST00000473695.1:n.99G=
NM_001306190.1:c.740G=	NP_001293119.1:p.Arg247=
NM_001698.2:c.827G= , LRG_449t1:c.827G=	NP_001689.1:p.Arg276=
XM_005252066.2:c.857G=	XP_005252123.1:p.Arg286=
XM_005252067.3:c.857G=	XP_005252124.1:p.Arg286=
XM_005252069.3:c.857G=	XP_005252126.1:p.Arg286=
XM_005252073.2:c.365G=	XP_005252130.1:p.Arg122=
XM_006717150.2:c.770G=	XP_006717213.1:p.Arg257=
XM_011518801.1:c.503G=	XP_011517103.1:p.Arg168=
XM_011518802.1:c.500G=	XP_011517104.1:p.Arg167=
NM_001351431.1:c.500G=	NP_001338360.1:p.Arg167=
NM_001351432.1:c.500G=	NP_001338361.1:p.Arg167=
NM_001351433.1:c.500G=	NP_001338362.1:p.Arg167=
XM_005252066.3:c.857G=	XP_005252123.1:p.Arg286=
XM_005252067.4:c.857G=	XP_005252124.1:p.Arg286=
XM_005252069.4:c.857G=	XP_005252126.1:p.Arg286=
XM_006717150.3:c.770G=	XP_006717213.1:p.Arg257=
XM_017014849.1:c.827G=	XP_016870338.1:p.Arg276=
XR_001746328.2:n.1052G=
XR_001746329.2:n.1004G=
NM_001698.3:c.827G= MANE Select	NP_001689.1:p.Arg276=
NM_001306190.2:c.740G=	NP_001293119.1:p.Arg247=
NM_001351431.2:c.500G=	NP_001338360.1:p.Arg167=
NM_001351432.2:c.500G=	NP_001338361.1:p.Arg167=
NM_001351433.2:c.500G=	NP_001338362.1:p.Arg167=