Canonical Allele Identifier: CA466225956

Gene: AUH

Linked Data

• MyVariant Identifiers: chr9:g.93983252G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220970G>C , CM000671.2:g.91220970G>C	GRCh38
NC_000009.11:g.93983252G>C , CM000671.1:g.93983252G>C	GRCh37
NC_000009.10:g.93023073G>C	NCBI36
NG_008017.1:g.145955C>G , LRG_449:g.145955C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.678C>G MANE Select	ENSP00000364883.5:p.Arg226=
ENST00000303617.5:c.591C>G	ENSP00000307334.5:p.Arg197=
ENST00000375731.8:c.678C>G	ENSP00000364883.4:p.Arg226=
NM_001306190.1:c.591C>G	NP_001293119.1:p.Arg197=
NM_001698.2:c.678C>G , LRG_449t1:c.678C>G	NP_001689.1:p.Arg226=
XM_005252066.2:c.708C>G	XP_005252123.1:p.Arg236=
XM_005252067.3:c.708C>G	XP_005252124.1:p.Arg236=
XM_005252069.3:c.708C>G	XP_005252126.1:p.Arg236=
XM_005252073.2:c.216C>G	XP_005252130.1:p.Arg72=
XM_006717150.2:c.621C>G	XP_006717213.1:p.Arg207=
XM_011518801.1:c.354C>G	XP_011517103.1:p.Arg118=
XM_011518802.1:c.351C>G	XP_011517104.1:p.Arg117=
NM_001351431.1:c.351C>G	NP_001338360.1:p.Arg117=
NM_001351432.1:c.351C>G	NP_001338361.1:p.Arg117=
NM_001351433.1:c.351C>G	NP_001338362.1:p.Arg117=
XM_005252066.3:c.708C>G	XP_005252123.1:p.Arg236=
XM_005252067.4:c.708C>G	XP_005252124.1:p.Arg236=
XM_005252069.4:c.708C>G	XP_005252126.1:p.Arg236=
XM_006717150.3:c.621C>G	XP_006717213.1:p.Arg207=
XM_017014849.1:c.678C>G	XP_016870338.1:p.Arg226=
XR_001746328.2:n.903C>G
XR_001746329.2:n.855C>G
NM_001698.3:c.678C>G MANE Select	NP_001689.1:p.Arg226=
NM_001306190.2:c.591C>G	NP_001293119.1:p.Arg197=
NM_001351431.2:c.351C>G	NP_001338360.1:p.Arg117=
NM_001351432.2:c.351C>G	NP_001338361.1:p.Arg117=
NM_001351433.2:c.351C>G	NP_001338362.1:p.Arg117=