Canonical Allele Identifier: CA2690635630

Gene: AUH

Linked Data

• gnomAD v4: 9-91220986-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220987del , CM000671.2:g.91220987del	GRCh38
NC_000009.11:g.93983269del , CM000671.1:g.93983269del	GRCh37
NC_000009.10:g.93023090del	NCBI36
NG_008017.1:g.145938del , LRG_449:g.145938del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.661del MANE Select	ENSP00000364883.5:p.Thr221HisfsTer?
ENST00000303617.5:c.574del	ENSP00000307334.5:p.Thr192HisfsTer?
ENST00000375731.8:c.661del	ENSP00000364883.4:p.Thr221HisfsTer?
NM_001306190.1:c.574del	NP_001293119.1:p.Thr192HisfsTer?
NM_001698.2:c.661del , LRG_449t1:c.661del	NP_001689.1:p.Thr221HisfsTer?
XM_005252066.2:c.691del	XP_005252123.1:p.Thr231HisfsTer?
XM_005252067.3:c.691del	XP_005252124.1:p.Thr231HisfsTer?
XM_005252069.3:c.691del	XP_005252126.1:p.Thr231HisfsTer?
XM_005252073.2:c.199del	XP_005252130.1:p.Thr67HisfsTer?
XM_006717150.2:c.604del	XP_006717213.1:p.Thr202HisfsTer?
XM_011518801.1:c.337del	XP_011517103.1:p.Thr113HisfsTer?
XM_011518802.1:c.334del	XP_011517104.1:p.Thr112HisfsTer?
NM_001351431.1:c.334del	NP_001338360.1:p.Thr112HisfsTer?
NM_001351432.1:c.334del	NP_001338361.1:p.Thr112HisfsTer?
NM_001351433.1:c.334del	NP_001338362.1:p.Thr112HisfsTer?
XM_005252066.3:c.691del	XP_005252123.1:p.Thr231HisfsTer?
XM_005252067.4:c.691del	XP_005252124.1:p.Thr231HisfsTer?
XM_005252069.4:c.691del	XP_005252126.1:p.Thr231HisfsTer?
XM_006717150.3:c.604del	XP_006717213.1:p.Thr202HisfsTer?
XM_017014849.1:c.661del	XP_016870338.1:p.Thr221HisfsTer?
XR_001746328.2:n.886del
XR_001746329.2:n.838del
NM_001698.3:c.661del MANE Select	NP_001689.1:p.Thr221HisfsTer?
NM_001306190.2:c.574del	NP_001293119.1:p.Thr192HisfsTer?
NM_001351431.2:c.334del	NP_001338360.1:p.Thr112HisfsTer?
NM_001351432.2:c.334del	NP_001338361.1:p.Thr112HisfsTer?
NM_001351433.2:c.334del	NP_001338362.1:p.Thr112HisfsTer?