Canonical Allele Identifier: CA373835280

Gene: AUH

Linked Data

• MyVariant Identifiers: chr9:g.93983225C>A (hg19) ; chr9:g.91220943C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220943C>A , CM000671.2:g.91220943C>A	GRCh38
NC_000009.11:g.93983225C>A , CM000671.1:g.93983225C>A	GRCh37
NC_000009.10:g.93023046C>A	NCBI36
NG_008017.1:g.145982G>T , LRG_449:g.145982G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.705G>T MANE Select	ENSP00000364883.5:p.Glu235Asp
ENST00000303617.5:c.618G>T	ENSP00000307334.5:p.Glu206Asp
ENST00000375731.8:c.705G>T	ENSP00000364883.4:p.Glu235Asp
NM_001306190.1:c.618G>T	NP_001293119.1:p.Glu206Asp
NM_001698.2:c.705G>T , LRG_449t1:c.705G>T	NP_001689.1:p.Glu235Asp
XM_005252066.2:c.735G>T	XP_005252123.1:p.Glu245Asp
XM_005252067.3:c.735G>T	XP_005252124.1:p.Glu245Asp
XM_005252069.3:c.735G>T	XP_005252126.1:p.Glu245Asp
XM_005252073.2:c.243G>T	XP_005252130.1:p.Glu81Asp
XM_006717150.2:c.648G>T	XP_006717213.1:p.Glu216Asp
XM_011518801.1:c.381G>T	XP_011517103.1:p.Glu127Asp
XM_011518802.1:c.378G>T	XP_011517104.1:p.Glu126Asp
NM_001351431.1:c.378G>T	NP_001338360.1:p.Glu126Asp
NM_001351432.1:c.378G>T	NP_001338361.1:p.Glu126Asp
NM_001351433.1:c.378G>T	NP_001338362.1:p.Glu126Asp
XM_005252066.3:c.735G>T	XP_005252123.1:p.Glu245Asp
XM_005252067.4:c.735G>T	XP_005252124.1:p.Glu245Asp
XM_005252069.4:c.735G>T	XP_005252126.1:p.Glu245Asp
XM_006717150.3:c.648G>T	XP_006717213.1:p.Glu216Asp
XM_017014849.1:c.705G>T	XP_016870338.1:p.Glu235Asp
XR_001746328.2:n.930G>T
XR_001746329.2:n.882G>T
NM_001698.3:c.705G>T MANE Select	NP_001689.1:p.Glu235Asp
NM_001306190.2:c.618G>T	NP_001293119.1:p.Glu206Asp
NM_001351431.2:c.378G>T	NP_001338360.1:p.Glu126Asp
NM_001351432.2:c.378G>T	NP_001338361.1:p.Glu126Asp
NM_001351433.2:c.378G>T	NP_001338362.1:p.Glu126Asp