Canonical Allele Identifier: CA373835032

Gene: AUH

Linked Data

• MyVariant Identifiers: chr9:g.93983107C>G (hg19) ; chr9:g.91220825C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220825C>G , CM000671.2:g.91220825C>G	GRCh38
NC_000009.11:g.93983107C>G , CM000671.1:g.93983107C>G	GRCh37
NC_000009.10:g.93022928C>G	NCBI36
NG_008017.1:g.146100G>C , LRG_449:g.146100G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.823G>C MANE Select	ENSP00000364883.5:p.Ala275Pro
ENST00000303617.5:c.736G>C	ENSP00000307334.5:p.Ala246Pro
ENST00000375731.8:c.823G>C	ENSP00000364883.4:p.Ala275Pro
ENST00000473695.1:n.95G>C
NM_001306190.1:c.736G>C	NP_001293119.1:p.Ala246Pro
NM_001698.2:c.823G>C , LRG_449t1:c.823G>C	NP_001689.1:p.Ala275Pro
XM_005252066.2:c.853G>C	XP_005252123.1:p.Ala285Pro
XM_005252067.3:c.853G>C	XP_005252124.1:p.Ala285Pro
XM_005252069.3:c.853G>C	XP_005252126.1:p.Ala285Pro
XM_005252073.2:c.361G>C	XP_005252130.1:p.Ala121Pro
XM_006717150.2:c.766G>C	XP_006717213.1:p.Ala256Pro
XM_011518801.1:c.499G>C	XP_011517103.1:p.Ala167Pro
XM_011518802.1:c.496G>C	XP_011517104.1:p.Ala166Pro
NM_001351431.1:c.496G>C	NP_001338360.1:p.Ala166Pro
NM_001351432.1:c.496G>C	NP_001338361.1:p.Ala166Pro
NM_001351433.1:c.496G>C	NP_001338362.1:p.Ala166Pro
XM_005252066.3:c.853G>C	XP_005252123.1:p.Ala285Pro
XM_005252067.4:c.853G>C	XP_005252124.1:p.Ala285Pro
XM_005252069.4:c.853G>C	XP_005252126.1:p.Ala285Pro
XM_006717150.3:c.766G>C	XP_006717213.1:p.Ala256Pro
XM_017014849.1:c.823G>C	XP_016870338.1:p.Ala275Pro
XR_001746328.2:n.1048G>C
XR_001746329.2:n.1000G>C
NM_001698.3:c.823G>C MANE Select	NP_001689.1:p.Ala275Pro
NM_001306190.2:c.736G>C	NP_001293119.1:p.Ala246Pro
NM_001351431.2:c.496G>C	NP_001338360.1:p.Ala166Pro
NM_001351432.2:c.496G>C	NP_001338361.1:p.Ala166Pro
NM_001351433.2:c.496G>C	NP_001338362.1:p.Ala166Pro