Canonical Allele Identifier: CA1863688873

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220816_91220818delinsACT , CM000671.2:g.91220816_91220818delinsACT	GRCh38
NC_000009.11:g.93983098_93983100delinsACT , CM000671.1:g.93983098_93983100delinsACT	GRCh37
NC_000009.10:g.93022919_93022921delinsACT	NCBI36
NG_008017.1:g.146107_146109delinsAGT , LRG_449:g.146107_146109delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.830_832delinsAGT MANE Select	ENSP00000364883.5:p.Glu277=
ENST00000303617.5:c.743_745delinsAGT	ENSP00000307334.5:p.Glu248=
ENST00000375731.8:c.830_832delinsAGT	ENSP00000364883.4:p.Glu277=
ENST00000473695.1:n.102_104delinsAGT
NM_001306190.1:c.743_745delinsAGT	NP_001293119.1:p.Glu248=
NM_001698.2:c.830_832delinsAGT , LRG_449t1:c.830_832delinsAGT	NP_001689.1:p.Glu277=
XM_005252066.2:c.860_862delinsAGT	XP_005252123.1:p.Glu287=
XM_005252067.3:c.860_862delinsAGT	XP_005252124.1:p.Glu287=
XM_005252069.3:c.860_862delinsAGT	XP_005252126.1:p.Glu287=
XM_005252073.2:c.368_370delinsAGT	XP_005252130.1:p.Glu123=
XM_006717150.2:c.773_775delinsAGT	XP_006717213.1:p.Glu258=
XM_011518801.1:c.506_508delinsAGT	XP_011517103.1:p.Glu169=
XM_011518802.1:c.503_505delinsAGT	XP_011517104.1:p.Glu168=
NM_001351431.1:c.503_505delinsAGT	NP_001338360.1:p.Glu168=
NM_001351432.1:c.503_505delinsAGT	NP_001338361.1:p.Glu168=
NM_001351433.1:c.503_505delinsAGT	NP_001338362.1:p.Glu168=
XM_005252066.3:c.860_862delinsAGT	XP_005252123.1:p.Glu287=
XM_005252067.4:c.860_862delinsAGT	XP_005252124.1:p.Glu287=
XM_005252069.4:c.860_862delinsAGT	XP_005252126.1:p.Glu287=
XM_006717150.3:c.773_775delinsAGT	XP_006717213.1:p.Glu258=
XM_017014849.1:c.830_832delinsAGT	XP_016870338.1:p.Glu277=
XR_001746328.2:n.1055_1057delinsAGT
XR_001746329.2:n.1007_1009delinsAGT
NM_001698.3:c.830_832delinsAGT MANE Select	NP_001689.1:p.Glu277=
NM_001306190.2:c.743_745delinsAGT	NP_001293119.1:p.Glu248=
NM_001351431.2:c.503_505delinsAGT	NP_001338360.1:p.Glu168=
NM_001351432.2:c.503_505delinsAGT	NP_001338361.1:p.Glu168=
NM_001351433.2:c.503_505delinsAGT	NP_001338362.1:p.Glu168=