Canonical Allele Identifier: CA1863731813

Gene: AUH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91356156_91356160delinsCTAGT , CM000671.2:g.91356156_91356160delinsCTAGT	GRCh38
NC_000009.11:g.94118438_94118442delinsCTAGT , CM000671.1:g.94118438_94118442delinsCTAGT	GRCh37
NC_000009.10:g.93158259_93158263delinsCTAGT	NCBI36
NG_008017.1:g.10765_10769delinsACTAG , LRG_449:g.10765_10769delinsACTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.263-5_263-1delinsACTAG MANE Select	ENSP00000364883.5:n.263-5_263-1delinsACTAG
ENST00000303617.5:c.263-5_263-1delinsACTAG	ENSP00000307334.5:n.263-5_263-1delinsACTAG
ENST00000375731.8:c.263-5_263-1delinsACTAG	ENSP00000364883.4:n.263-5_263-1delinsACTAG
ENST00000478465.5:n.423-5_423-1delinsACTAG
NM_001306190.1:c.263-5_263-1delinsACTAG	NP_001293119.1:n.263-5_263-1delinsACTAG
NM_001698.2:c.263-5_263-1delinsACTAG , LRG_449t1:c.263-5_263-1delinsACTAG	NP_001689.1:n.263-5_263-1delinsACTAG
XM_005252066.2:c.293-5_293-1delinsACTAG	XP_005252123.1:n.293-5_293-1delinsACTAG
XM_005252067.3:c.293-5_293-1delinsACTAG	XP_005252124.1:n.293-5_293-1delinsACTAG
XM_005252069.3:c.293-5_293-1delinsACTAG	XP_005252126.1:n.293-5_293-1delinsACTAG
XM_005252072.1:c.263-5_263-1delinsACTAG	XP_005252129.1:n.263-5_263-1delinsACTAG
XM_006717150.2:c.293-5_293-1delinsACTAG	XP_006717213.1:n.293-5_293-1delinsACTAG
XM_011518800.1:c.293-5_293-1delinsACTAG	XP_011517102.1:n.293-5_293-1delinsACTAG
XM_011518802.1:c.-65-5_-65-1delinsACTAG	XP_011517104.1:n.-65-5_-65-1delinsACTAG
XM_011518803.1:c.293-5_293-1delinsACTAG	XP_011517105.1:n.293-5_293-1delinsACTAG
XM_011518804.1:c.263-5_263-1delinsACTAG	XP_011517106.1:n.263-5_263-1delinsACTAG
XR_929814.1:n.343-5_343-1delinsACTAG
NM_001351431.1:c.-65-5_-65-1delinsACTAG	NP_001338360.1:n.-65-5_-65-1delinsACTAG
NM_001351432.1:c.-65-5_-65-1delinsACTAG	NP_001338361.1:n.-65-5_-65-1delinsACTAG
NM_001351433.1:c.-65-5_-65-1delinsACTAG	NP_001338362.1:n.-65-5_-65-1delinsACTAG
XM_005252066.3:c.293-5_293-1delinsACTAG	XP_005252123.1:n.293-5_293-1delinsACTAG
XM_005252067.4:c.293-5_293-1delinsACTAG	XP_005252124.1:n.293-5_293-1delinsACTAG
XM_005252069.4:c.293-5_293-1delinsACTAG	XP_005252126.1:n.293-5_293-1delinsACTAG
XM_005252072.2:c.263-5_263-1delinsACTAG	XP_005252129.1:n.263-5_263-1delinsACTAG
XM_006717150.3:c.293-5_293-1delinsACTAG	XP_006717213.1:n.293-5_293-1delinsACTAG
XM_011518800.3:c.293-5_293-1delinsACTAG	XP_011517102.1:n.293-5_293-1delinsACTAG
XM_011518803.2:c.293-5_293-1delinsACTAG	XP_011517105.1:n.293-5_293-1delinsACTAG
XM_017014849.1:c.263-5_263-1delinsACTAG	XP_016870338.1:n.263-5_263-1delinsACTAG
XR_001746328.2:n.346-5_346-1delinsACTAG
XR_001746329.2:n.298-5_298-1delinsACTAG
NM_001698.3:c.263-5_263-1delinsACTAG MANE Select	NP_001689.1:n.263-5_263-1delinsACTAG
NM_001306190.2:c.263-5_263-1delinsACTAG	NP_001293119.1:n.263-5_263-1delinsACTAG
NM_001351431.2:c.-65-5_-65-1delinsACTAG	NP_001338360.1:n.-65-5_-65-1delinsACTAG
NM_001351432.2:c.-65-5_-65-1delinsACTAG	NP_001338361.1:n.-65-5_-65-1delinsACTAG
NM_001351433.2:c.-65-5_-65-1delinsACTAG	NP_001338362.1:n.-65-5_-65-1delinsACTAG