Canonical Allele Identifier: CA466225946

Gene: AUH

Linked Data

• MyVariant Identifiers: chr9:g.93983249G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220967G>T , CM000671.2:g.91220967G>T	GRCh38
NC_000009.11:g.93983249G>T , CM000671.1:g.93983249G>T	GRCh37
NC_000009.10:g.93023070G>T	NCBI36
NG_008017.1:g.145958C>A , LRG_449:g.145958C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.681C>A MANE Select	ENSP00000364883.5:p.Ala227=
ENST00000303617.5:c.594C>A	ENSP00000307334.5:p.Ala198=
ENST00000375731.8:c.681C>A	ENSP00000364883.4:p.Ala227=
NM_001306190.1:c.594C>A	NP_001293119.1:p.Ala198=
NM_001698.2:c.681C>A , LRG_449t1:c.681C>A	NP_001689.1:p.Ala227=
XM_005252066.2:c.711C>A	XP_005252123.1:p.Ala237=
XM_005252067.3:c.711C>A	XP_005252124.1:p.Ala237=
XM_005252069.3:c.711C>A	XP_005252126.1:p.Ala237=
XM_005252073.2:c.219C>A	XP_005252130.1:p.Ala73=
XM_006717150.2:c.624C>A	XP_006717213.1:p.Ala208=
XM_011518801.1:c.357C>A	XP_011517103.1:p.Ala119=
XM_011518802.1:c.354C>A	XP_011517104.1:p.Ala118=
NM_001351431.1:c.354C>A	NP_001338360.1:p.Ala118=
NM_001351432.1:c.354C>A	NP_001338361.1:p.Ala118=
NM_001351433.1:c.354C>A	NP_001338362.1:p.Ala118=
XM_005252066.3:c.711C>A	XP_005252123.1:p.Ala237=
XM_005252067.4:c.711C>A	XP_005252124.1:p.Ala237=
XM_005252069.4:c.711C>A	XP_005252126.1:p.Ala237=
XM_006717150.3:c.624C>A	XP_006717213.1:p.Ala208=
XM_017014849.1:c.681C>A	XP_016870338.1:p.Ala227=
XR_001746328.2:n.906C>A
XR_001746329.2:n.858C>A
NM_001698.3:c.681C>A MANE Select	NP_001689.1:p.Ala227=
NM_001306190.2:c.594C>A	NP_001293119.1:p.Ala198=
NM_001351431.2:c.354C>A	NP_001338360.1:p.Ala118=
NM_001351432.2:c.354C>A	NP_001338361.1:p.Ala118=
NM_001351433.2:c.354C>A	NP_001338362.1:p.Ala118=