Canonical Allele Identifier: CA1752544946

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186485_151186506delinsACACAGGCAGTGTGGCCTGCAG , CM000669.2:g.151186485_151186506delinsACACAGGCAGTGTGGCCTGCAG	GRCh38
NC_000007.13:g.150883572_150883593delinsACACAGGCAGTGTGGCCTGCAG , CM000669.1:g.150883572_150883593delinsACACAGGCAGTGTGGCCTGCAG	GRCh37
NC_000007.12:g.150514505_150514526delinsACACAGGCAGTGTGGCCTGCAG	NCBI36
NG_017016.1:g.6327_6348delinsCTGCAGGCCACACTGCCTGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.470_491delinsCTGCAGGCCACACTGCCTGTGT MANE Select	ENSP00000391137.2:p.Ala157=
ENST00000275838.5:c.470_491delinsCTGCAGGCCACACTGCCTGTGT	ENSP00000275838.1:p.Ala157=
ENST00000377867.7:c.425_446delinsCTGCAGGCCACACTGCCTGTGT	ENSP00000367098.3:p.Ala142=
ENST00000420175.2:c.470_491delinsCTGCAGGCCACACTGCCTGTGT	ENSP00000391137.2:p.Ala157=
NM_001142459.1:c.470_491delinsCTGCAGGCCACACTGCCTGTGT	NP_001135931.2:p.Ala157=
NM_001142460.1:c.470_491delinsCTGCAGGCCACACTGCCTGTGT	NP_001135932.2:p.Ala157=
NM_080871.3:c.425_446delinsCTGCAGGCCACACTGCCTGTGT	NP_543147.2:p.Ala142=
XM_005249949.3:c.605_626delinsCTGCAGGCCACACTGCCTGTGT	XP_005250006.1:p.Ala202=
NM_001142459.2:c.470_491delinsCTGCAGGCCACACTGCCTGTGT MANE Select	NP_001135931.2:p.Ala157=
NM_080871.4:c.425_446delinsCTGCAGGCCACACTGCCTGTGT	NP_543147.2:p.Ala142=