Canonical Allele Identifier: CA373835025

Gene: AUH

Linked Data

• MyVariant Identifiers: chr9:g.93983103C>G (hg19) ; chr9:g.91220821C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220821C>G , CM000671.2:g.91220821C>G	GRCh38
NC_000009.11:g.93983103C>G , CM000671.1:g.93983103C>G	GRCh37
NC_000009.10:g.93022924C>G	NCBI36
NG_008017.1:g.146104G>C , LRG_449:g.146104G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.827G>C MANE Select	ENSP00000364883.5:p.Arg276Thr
ENST00000303617.5:c.740G>C	ENSP00000307334.5:p.Arg247Thr
ENST00000375731.8:c.827G>C	ENSP00000364883.4:p.Arg276Thr
ENST00000473695.1:n.99G>C
NM_001306190.1:c.740G>C	NP_001293119.1:p.Arg247Thr
NM_001698.2:c.827G>C , LRG_449t1:c.827G>C	NP_001689.1:p.Arg276Thr
XM_005252066.2:c.857G>C	XP_005252123.1:p.Arg286Thr
XM_005252067.3:c.857G>C	XP_005252124.1:p.Arg286Thr
XM_005252069.3:c.857G>C	XP_005252126.1:p.Arg286Thr
XM_005252073.2:c.365G>C	XP_005252130.1:p.Arg122Thr
XM_006717150.2:c.770G>C	XP_006717213.1:p.Arg257Thr
XM_011518801.1:c.503G>C	XP_011517103.1:p.Arg168Thr
XM_011518802.1:c.500G>C	XP_011517104.1:p.Arg167Thr
NM_001351431.1:c.500G>C	NP_001338360.1:p.Arg167Thr
NM_001351432.1:c.500G>C	NP_001338361.1:p.Arg167Thr
NM_001351433.1:c.500G>C	NP_001338362.1:p.Arg167Thr
XM_005252066.3:c.857G>C	XP_005252123.1:p.Arg286Thr
XM_005252067.4:c.857G>C	XP_005252124.1:p.Arg286Thr
XM_005252069.4:c.857G>C	XP_005252126.1:p.Arg286Thr
XM_006717150.3:c.770G>C	XP_006717213.1:p.Arg257Thr
XM_017014849.1:c.827G>C	XP_016870338.1:p.Arg276Thr
XR_001746328.2:n.1052G>C
XR_001746329.2:n.1004G>C
NM_001698.3:c.827G>C MANE Select	NP_001689.1:p.Arg276Thr
NM_001306190.2:c.740G>C	NP_001293119.1:p.Arg247Thr
NM_001351431.2:c.500G>C	NP_001338360.1:p.Arg167Thr
NM_001351432.2:c.500G>C	NP_001338361.1:p.Arg167Thr
NM_001351433.2:c.500G>C	NP_001338362.1:p.Arg167Thr