Canonical Allele Identifier: CA1863689321

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91221240A= , CM000671.2:g.91221240A=	GRCh38
NC_000009.11:g.93983522A= , CM000671.1:g.93983522A=	GRCh37
NC_000009.10:g.93023343A=	NCBI36
NG_008017.1:g.145685T= , LRG_449:g.145685T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.656-248T= MANE Select	ENSP00000364883.5:n.656-248T=
ENST00000303617.5:c.569-248T=	ENSP00000307334.5:n.569-248T=
ENST00000375731.8:c.656-248T=	ENSP00000364883.4:n.656-248T=
NM_001306190.1:c.569-248T=	NP_001293119.1:n.569-248T=
NM_001698.2:c.656-248T= , LRG_449t1:c.656-248T=	NP_001689.1:n.656-248T=
XM_005252066.2:c.686-248T=	XP_005252123.1:n.686-248T=
XM_005252067.3:c.686-248T=	XP_005252124.1:n.686-248T=
XM_005252069.3:c.686-248T=	XP_005252126.1:n.686-248T=
XM_005252073.2:c.194-248T=	XP_005252130.1:n.194-248T=
XM_006717150.2:c.599-248T=	XP_006717213.1:n.599-248T=
XM_011518801.1:c.332-248T=	XP_011517103.1:n.332-248T=
XM_011518802.1:c.329-248T=	XP_011517104.1:n.329-248T=
NM_001351431.1:c.329-248T=	NP_001338360.1:n.329-248T=
NM_001351432.1:c.329-248T=	NP_001338361.1:n.329-248T=
NM_001351433.1:c.329-248T=	NP_001338362.1:n.329-248T=
XM_005252066.3:c.686-248T=	XP_005252123.1:n.686-248T=
XM_005252067.4:c.686-248T=	XP_005252124.1:n.686-248T=
XM_005252069.4:c.686-248T=	XP_005252126.1:n.686-248T=
XM_006717150.3:c.599-248T=	XP_006717213.1:n.599-248T=
XM_017014849.1:c.656-248T=	XP_016870338.1:n.656-248T=
XR_001746328.2:n.881-248T=
XR_001746329.2:n.833-248T=
NM_001698.3:c.656-248T= MANE Select	NP_001689.1:n.656-248T=
NM_001306190.2:c.569-248T=	NP_001293119.1:n.569-248T=
NM_001351431.2:c.329-248T=	NP_001338360.1:n.329-248T=
NM_001351432.2:c.329-248T=	NP_001338361.1:n.329-248T=
NM_001351433.2:c.329-248T=	NP_001338362.1:n.329-248T=