Canonical Allele Identifier: CA1863688927

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220844G= , CM000671.2:g.91220844G=	GRCh38
NC_000009.11:g.93983126G= , CM000671.1:g.93983126G=	GRCh37
NC_000009.10:g.93022947G=	NCBI36
NG_008017.1:g.146081C= , LRG_449:g.146081C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.804C= MANE Select	ENSP00000364883.5:p.Tyr268=
ENST00000303617.5:c.717C=	ENSP00000307334.5:p.Tyr239=
ENST00000375731.8:c.804C=	ENSP00000364883.4:p.Tyr268=
ENST00000473695.1:n.76C=
NM_001306190.1:c.717C=	NP_001293119.1:p.Tyr239=
NM_001698.2:c.804C= , LRG_449t1:c.804C=	NP_001689.1:p.Tyr268=
XM_005252066.2:c.834C=	XP_005252123.1:p.Tyr278=
XM_005252067.3:c.834C=	XP_005252124.1:p.Tyr278=
XM_005252069.3:c.834C=	XP_005252126.1:p.Tyr278=
XM_005252073.2:c.342C=	XP_005252130.1:p.Tyr114=
XM_006717150.2:c.747C=	XP_006717213.1:p.Tyr249=
XM_011518801.1:c.480C=	XP_011517103.1:p.Tyr160=
XM_011518802.1:c.477C=	XP_011517104.1:p.Tyr159=
NM_001351431.1:c.477C=	NP_001338360.1:p.Tyr159=
NM_001351432.1:c.477C=	NP_001338361.1:p.Tyr159=
NM_001351433.1:c.477C=	NP_001338362.1:p.Tyr159=
XM_005252066.3:c.834C=	XP_005252123.1:p.Tyr278=
XM_005252067.4:c.834C=	XP_005252124.1:p.Tyr278=
XM_005252069.4:c.834C=	XP_005252126.1:p.Tyr278=
XM_006717150.3:c.747C=	XP_006717213.1:p.Tyr249=
XM_017014849.1:c.804C=	XP_016870338.1:p.Tyr268=
XR_001746328.2:n.1029C=
XR_001746329.2:n.981C=
NM_001698.3:c.804C= MANE Select	NP_001689.1:p.Tyr268=
NM_001306190.2:c.717C=	NP_001293119.1:p.Tyr239=
NM_001351431.2:c.477C=	NP_001338360.1:p.Tyr159=
NM_001351432.2:c.477C=	NP_001338361.1:p.Tyr159=
NM_001351433.2:c.477C=	NP_001338362.1:p.Tyr159=