Canonical Allele Identifier: CA1863688864

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220812A= , CM000671.2:g.91220812A=	GRCh38
NC_000009.11:g.93983094A= , CM000671.1:g.93983094A=	GRCh37
NC_000009.10:g.93022915A=	NCBI36
NG_008017.1:g.146113T= , LRG_449:g.146113T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.836T= MANE Select	ENSP00000364883.5:p.Leu279=
ENST00000303617.5:c.749T=	ENSP00000307334.5:p.Leu250=
ENST00000375731.8:c.836T=	ENSP00000364883.4:p.Leu279=
ENST00000473695.1:n.108T=
NM_001306190.1:c.749T=	NP_001293119.1:p.Leu250=
NM_001698.2:c.836T= , LRG_449t1:c.836T=	NP_001689.1:p.Leu279=
XM_005252066.2:c.866T=	XP_005252123.1:p.Leu289=
XM_005252067.3:c.866T=	XP_005252124.1:p.Leu289=
XM_005252069.3:c.866T=	XP_005252126.1:p.Leu289=
XM_005252073.2:c.374T=	XP_005252130.1:p.Leu125=
XM_006717150.2:c.779T=	XP_006717213.1:p.Leu260=
XM_011518801.1:c.512T=	XP_011517103.1:p.Leu171=
XM_011518802.1:c.509T=	XP_011517104.1:p.Leu170=
NM_001351431.1:c.509T=	NP_001338360.1:p.Leu170=
NM_001351432.1:c.509T=	NP_001338361.1:p.Leu170=
NM_001351433.1:c.509T=	NP_001338362.1:p.Leu170=
XM_005252066.3:c.866T=	XP_005252123.1:p.Leu289=
XM_005252067.4:c.866T=	XP_005252124.1:p.Leu289=
XM_005252069.4:c.866T=	XP_005252126.1:p.Leu289=
XM_006717150.3:c.779T=	XP_006717213.1:p.Leu260=
XM_017014849.1:c.836T=	XP_016870338.1:p.Leu279=
XR_001746328.2:n.1061T=
XR_001746329.2:n.1013T=
NM_001698.3:c.836T= MANE Select	NP_001689.1:p.Leu279=
NM_001306190.2:c.749T=	NP_001293119.1:p.Leu250=
NM_001351431.2:c.509T=	NP_001338360.1:p.Leu170=
NM_001351432.2:c.509T=	NP_001338361.1:p.Leu170=
NM_001351433.2:c.509T=	NP_001338362.1:p.Leu170=