Canonical Allele Identifier: CA2785064711

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220986_91220987insACA , CM000671.2:g.91220986_91220987insACA	GRCh38
NC_000009.11:g.93983268_93983269insACA , CM000671.1:g.93983268_93983269insACA	GRCh37
NC_000009.10:g.93023089_93023090insACA	NCBI36
NG_008017.1:g.145938_145939insTGT , LRG_449:g.145938_145939insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.661_662insTGT MANE Select	ENSP00000364883.5:p.Thr221delinsMetSer
ENST00000303617.5:c.574_575insTGT	ENSP00000307334.5:p.Thr192delinsMetSer
ENST00000375731.8:c.661_662insTGT	ENSP00000364883.4:p.Thr221delinsMetSer
NM_001306190.1:c.574_575insTGT	NP_001293119.1:p.Thr192delinsMetSer
NM_001698.2:c.661_662insTGT , LRG_449t1:c.661_662insTGT	NP_001689.1:p.Thr221delinsMetSer
XM_005252066.2:c.691_692insTGT	XP_005252123.1:p.Thr231delinsMetSer
XM_005252067.3:c.691_692insTGT	XP_005252124.1:p.Thr231delinsMetSer
XM_005252069.3:c.691_692insTGT	XP_005252126.1:p.Thr231delinsMetSer
XM_005252073.2:c.199_200insTGT	XP_005252130.1:p.Thr67delinsMetSer
XM_006717150.2:c.604_605insTGT	XP_006717213.1:p.Thr202delinsMetSer
XM_011518801.1:c.337_338insTGT	XP_011517103.1:p.Thr113delinsMetSer
XM_011518802.1:c.334_335insTGT	XP_011517104.1:p.Thr112delinsMetSer
NM_001351431.1:c.334_335insTGT	NP_001338360.1:p.Thr112delinsMetSer
NM_001351432.1:c.334_335insTGT	NP_001338361.1:p.Thr112delinsMetSer
NM_001351433.1:c.334_335insTGT	NP_001338362.1:p.Thr112delinsMetSer
XM_005252066.3:c.691_692insTGT	XP_005252123.1:p.Thr231delinsMetSer
XM_005252067.4:c.691_692insTGT	XP_005252124.1:p.Thr231delinsMetSer
XM_005252069.4:c.691_692insTGT	XP_005252126.1:p.Thr231delinsMetSer
XM_006717150.3:c.604_605insTGT	XP_006717213.1:p.Thr202delinsMetSer
XM_017014849.1:c.661_662insTGT	XP_016870338.1:p.Thr221delinsMetSer
XR_001746328.2:n.886_887insTGT
XR_001746329.2:n.838_839insTGT
NM_001698.3:c.661_662insTGT MANE Select	NP_001689.1:p.Thr221delinsMetSer
NM_001306190.2:c.574_575insTGT	NP_001293119.1:p.Thr192delinsMetSer
NM_001351431.2:c.334_335insTGT	NP_001338360.1:p.Thr112delinsMetSer
NM_001351432.2:c.334_335insTGT	NP_001338361.1:p.Thr112delinsMetSer
NM_001351433.2:c.334_335insTGT	NP_001338362.1:p.Thr112delinsMetSer