Canonical Allele Identifier: CA373835126

Gene: AUH

Linked Data

• MyVariant Identifiers: chr9:g.93983151T>G (hg19) ; chr9:g.91220869T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220869T>G , CM000671.2:g.91220869T>G	GRCh38
NC_000009.11:g.93983151T>G , CM000671.1:g.93983151T>G	GRCh37
NC_000009.10:g.93022972T>G	NCBI36
NG_008017.1:g.146056A>C , LRG_449:g.146056A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.779A>C MANE Select	ENSP00000364883.5:p.Gln260Pro
ENST00000303617.5:c.692A>C	ENSP00000307334.5:p.Gln231Pro
ENST00000375731.8:c.779A>C	ENSP00000364883.4:p.Gln260Pro
ENST00000473695.1:n.51A>C
NM_001306190.1:c.692A>C	NP_001293119.1:p.Gln231Pro
NM_001698.2:c.779A>C , LRG_449t1:c.779A>C	NP_001689.1:p.Gln260Pro
XM_005252066.2:c.809A>C	XP_005252123.1:p.Gln270Pro
XM_005252067.3:c.809A>C	XP_005252124.1:p.Gln270Pro
XM_005252069.3:c.809A>C	XP_005252126.1:p.Gln270Pro
XM_005252073.2:c.317A>C	XP_005252130.1:p.Gln106Pro
XM_006717150.2:c.722A>C	XP_006717213.1:p.Gln241Pro
XM_011518801.1:c.455A>C	XP_011517103.1:p.Gln152Pro
XM_011518802.1:c.452A>C	XP_011517104.1:p.Gln151Pro
NM_001351431.1:c.452A>C	NP_001338360.1:p.Gln151Pro
NM_001351432.1:c.452A>C	NP_001338361.1:p.Gln151Pro
NM_001351433.1:c.452A>C	NP_001338362.1:p.Gln151Pro
XM_005252066.3:c.809A>C	XP_005252123.1:p.Gln270Pro
XM_005252067.4:c.809A>C	XP_005252124.1:p.Gln270Pro
XM_005252069.4:c.809A>C	XP_005252126.1:p.Gln270Pro
XM_006717150.3:c.722A>C	XP_006717213.1:p.Gln241Pro
XM_017014849.1:c.779A>C	XP_016870338.1:p.Gln260Pro
XR_001746328.2:n.1004A>C
XR_001746329.2:n.956A>C
NM_001698.3:c.779A>C MANE Select	NP_001689.1:p.Gln260Pro
NM_001306190.2:c.692A>C	NP_001293119.1:p.Gln231Pro
NM_001351431.2:c.452A>C	NP_001338360.1:p.Gln151Pro
NM_001351432.2:c.452A>C	NP_001338361.1:p.Gln151Pro
NM_001351433.2:c.452A>C	NP_001338362.1:p.Gln151Pro