Canonical Allele Identifier: CA373836863

Gene: AUH

Linked Data

• dbSNP Id: rs931179337
• MyVariant Identifiers: chr9:g.94060281C>A (hg19) ; chr9:g.91297999C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91297999C>A , CM000671.2:g.91297999C>A	GRCh38
NC_000009.11:g.94060281C>A , CM000671.1:g.94060281C>A	GRCh37
NC_000009.10:g.93100102C>A	NCBI36
NG_008017.1:g.68926G>T , LRG_449:g.68926G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375731.9:c.583G>T MANE Select	ENSP00000364883.5:p.Asp195Tyr
ENST00000303617.5:c.496G>T	ENSP00000307334.5:p.Asp166Tyr
ENST00000375731.8:c.583G>T	ENSP00000364883.4:p.Asp195Tyr
ENST00000478465.5:n.743G>T
NM_001306190.1:c.496G>T	NP_001293119.1:p.Asp166Tyr
NM_001698.2:c.583G>T , LRG_449t1:c.583G>T	NP_001689.1:p.Asp195Tyr
XM_005252066.2:c.613G>T	XP_005252123.1:p.Asp205Tyr
XM_005252067.3:c.613G>T	XP_005252124.1:p.Asp205Tyr
XM_005252069.3:c.613G>T	XP_005252126.1:p.Asp205Tyr
XM_005252072.1:c.583G>T	XP_005252129.1:p.Asp195Tyr
XM_005252073.2:c.121G>T	XP_005252130.1:p.Asp41Tyr
XM_006717150.2:c.526G>T	XP_006717213.1:p.Asp176Tyr
XM_011518800.1:c.613G>T	XP_011517102.1:p.Asp205Tyr
XM_011518801.1:c.259G>T	XP_011517103.1:p.Asp87Tyr
XM_011518802.1:c.256G>T	XP_011517104.1:p.Asp86Tyr
NM_001351431.1:c.256G>T	NP_001338360.1:p.Asp86Tyr
NM_001351432.1:c.256G>T	NP_001338361.1:p.Asp86Tyr
NM_001351433.1:c.256G>T	NP_001338362.1:p.Asp86Tyr
XM_005252066.3:c.613G>T	XP_005252123.1:p.Asp205Tyr
XM_005252067.4:c.613G>T	XP_005252124.1:p.Asp205Tyr
XM_005252069.4:c.613G>T	XP_005252126.1:p.Asp205Tyr
XM_005252072.2:c.583G>T	XP_005252129.1:p.Asp195Tyr
XM_006717150.3:c.526G>T	XP_006717213.1:p.Asp176Tyr
XM_011518800.3:c.613G>T	XP_011517102.1:p.Asp205Tyr
XM_017014849.1:c.583G>T	XP_016870338.1:p.Asp195Tyr
XR_001746328.2:n.666G>T
XR_001746329.2:n.618G>T
NM_001698.3:c.583G>T MANE Select	NP_001689.1:p.Asp195Tyr
NM_001306190.2:c.496G>T	NP_001293119.1:p.Asp166Tyr
NM_001351431.2:c.256G>T	NP_001338360.1:p.Asp86Tyr
NM_001351432.2:c.256G>T	NP_001338361.1:p.Asp86Tyr
NM_001351433.2:c.256G>T	NP_001338362.1:p.Asp86Tyr