Canonical Allele Identifier: CA466225965

Gene: AUH

Linked Data

• MyVariant Identifiers: chr9:g.93983255T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220973T>A , CM000671.2:g.91220973T>A	GRCh38
NC_000009.11:g.93983255T>A , CM000671.1:g.93983255T>A	GRCh37
NC_000009.10:g.93023076T>A	NCBI36
NG_008017.1:g.145952A>T , LRG_449:g.145952A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.675A>T MANE Select	ENSP00000364883.5:p.Pro225=
ENST00000303617.5:c.588A>T	ENSP00000307334.5:p.Pro196=
ENST00000375731.8:c.675A>T	ENSP00000364883.4:p.Pro225=
NM_001306190.1:c.588A>T	NP_001293119.1:p.Pro196=
NM_001698.2:c.675A>T , LRG_449t1:c.675A>T	NP_001689.1:p.Pro225=
XM_005252066.2:c.705A>T	XP_005252123.1:p.Pro235=
XM_005252067.3:c.705A>T	XP_005252124.1:p.Pro235=
XM_005252069.3:c.705A>T	XP_005252126.1:p.Pro235=
XM_005252073.2:c.213A>T	XP_005252130.1:p.Pro71=
XM_006717150.2:c.618A>T	XP_006717213.1:p.Pro206=
XM_011518801.1:c.351A>T	XP_011517103.1:p.Pro117=
XM_011518802.1:c.348A>T	XP_011517104.1:p.Pro116=
NM_001351431.1:c.348A>T	NP_001338360.1:p.Pro116=
NM_001351432.1:c.348A>T	NP_001338361.1:p.Pro116=
NM_001351433.1:c.348A>T	NP_001338362.1:p.Pro116=
XM_005252066.3:c.705A>T	XP_005252123.1:p.Pro235=
XM_005252067.4:c.705A>T	XP_005252124.1:p.Pro235=
XM_005252069.4:c.705A>T	XP_005252126.1:p.Pro235=
XM_006717150.3:c.618A>T	XP_006717213.1:p.Pro206=
XM_017014849.1:c.675A>T	XP_016870338.1:p.Pro225=
XR_001746328.2:n.900A>T
XR_001746329.2:n.852A>T
NM_001698.3:c.675A>T MANE Select	NP_001689.1:p.Pro225=
NM_001306190.2:c.588A>T	NP_001293119.1:p.Pro196=
NM_001351431.2:c.348A>T	NP_001338360.1:p.Pro116=
NM_001351432.2:c.348A>T	NP_001338361.1:p.Pro116=
NM_001351433.2:c.348A>T	NP_001338362.1:p.Pro116=