Canonical Allele Identifier: CA1863689122

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220974G= , CM000671.2:g.91220974G=	GRCh38
NC_000009.11:g.93983256G= , CM000671.1:g.93983256G=	GRCh37
NC_000009.10:g.93023077G=	NCBI36
NG_008017.1:g.145951C= , LRG_449:g.145951C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.674C= MANE Select	ENSP00000364883.5:p.Pro225=
ENST00000303617.5:c.587C=	ENSP00000307334.5:p.Pro196=
ENST00000375731.8:c.674C=	ENSP00000364883.4:p.Pro225=
NM_001306190.1:c.587C=	NP_001293119.1:p.Pro196=
NM_001698.2:c.674C= , LRG_449t1:c.674C=	NP_001689.1:p.Pro225=
XM_005252066.2:c.704C=	XP_005252123.1:p.Pro235=
XM_005252067.3:c.704C=	XP_005252124.1:p.Pro235=
XM_005252069.3:c.704C=	XP_005252126.1:p.Pro235=
XM_005252073.2:c.212C=	XP_005252130.1:p.Pro71=
XM_006717150.2:c.617C=	XP_006717213.1:p.Pro206=
XM_011518801.1:c.350C=	XP_011517103.1:p.Pro117=
XM_011518802.1:c.347C=	XP_011517104.1:p.Pro116=
NM_001351431.1:c.347C=	NP_001338360.1:p.Pro116=
NM_001351432.1:c.347C=	NP_001338361.1:p.Pro116=
NM_001351433.1:c.347C=	NP_001338362.1:p.Pro116=
XM_005252066.3:c.704C=	XP_005252123.1:p.Pro235=
XM_005252067.4:c.704C=	XP_005252124.1:p.Pro235=
XM_005252069.4:c.704C=	XP_005252126.1:p.Pro235=
XM_006717150.3:c.617C=	XP_006717213.1:p.Pro206=
XM_017014849.1:c.674C=	XP_016870338.1:p.Pro225=
XR_001746328.2:n.899C=
XR_001746329.2:n.851C=
NM_001698.3:c.674C= MANE Select	NP_001689.1:p.Pro225=
NM_001306190.2:c.587C=	NP_001293119.1:p.Pro196=
NM_001351431.2:c.347C=	NP_001338360.1:p.Pro116=
NM_001351432.2:c.347C=	NP_001338361.1:p.Pro116=
NM_001351433.2:c.347C=	NP_001338362.1:p.Pro116=