Canonical Allele Identifier: CA466225474

Gene: AUH

Linked Data

• MyVariant Identifiers: chr9:g.93983090A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220808A>G , CM000671.2:g.91220808A>G	GRCh38
NC_000009.11:g.93983090A>G , CM000671.1:g.93983090A>G	GRCh37
NC_000009.10:g.93022911A>G	NCBI36
NG_008017.1:g.146117T>C , LRG_449:g.146117T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.840T>C MANE Select	ENSP00000364883.5:p.Pro280=
ENST00000303617.5:c.753T>C	ENSP00000307334.5:p.Pro251=
ENST00000375731.8:c.840T>C	ENSP00000364883.4:p.Pro280=
ENST00000473695.1:n.112T>C
NM_001306190.1:c.753T>C	NP_001293119.1:p.Pro251=
NM_001698.2:c.840T>C , LRG_449t1:c.840T>C	NP_001689.1:p.Pro280=
XM_005252066.2:c.870T>C	XP_005252123.1:p.Pro290=
XM_005252067.3:c.870T>C	XP_005252124.1:p.Pro290=
XM_005252069.3:c.870T>C	XP_005252126.1:p.Pro290=
XM_005252073.2:c.378T>C	XP_005252130.1:p.Pro126=
XM_006717150.2:c.783T>C	XP_006717213.1:p.Pro261=
XM_011518801.1:c.516T>C	XP_011517103.1:p.Pro172=
XM_011518802.1:c.513T>C	XP_011517104.1:p.Pro171=
NM_001351431.1:c.513T>C	NP_001338360.1:p.Pro171=
NM_001351432.1:c.513T>C	NP_001338361.1:p.Pro171=
NM_001351433.1:c.513T>C	NP_001338362.1:p.Pro171=
XM_005252066.3:c.870T>C	XP_005252123.1:p.Pro290=
XM_005252067.4:c.870T>C	XP_005252124.1:p.Pro290=
XM_005252069.4:c.870T>C	XP_005252126.1:p.Pro290=
XM_006717150.3:c.783T>C	XP_006717213.1:p.Pro261=
XM_017014849.1:c.840T>C	XP_016870338.1:p.Pro280=
XR_001746328.2:n.1065T>C
XR_001746329.2:n.1017T>C
NM_001698.3:c.840T>C MANE Select	NP_001689.1:p.Pro280=
NM_001306190.2:c.753T>C	NP_001293119.1:p.Pro251=
NM_001351431.2:c.513T>C	NP_001338360.1:p.Pro171=
NM_001351432.2:c.513T>C	NP_001338361.1:p.Pro171=
NM_001351433.2:c.513T>C	NP_001338362.1:p.Pro171=