Canonical Allele Identifier: CA1752545075

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186538_151186539delinsAG , CM000669.2:g.151186538_151186539delinsAG	GRCh38
NC_000007.13:g.150883625_150883626delinsAG , CM000669.1:g.150883625_150883626delinsAG	GRCh37
NC_000007.12:g.150514558_150514559delinsAG	NCBI36
NG_017016.1:g.6294_6295delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.437_438delinsCT MANE Select	ENSP00000391137.2:p.Pro146=
ENST00000275838.5:c.437_438delinsCT	ENSP00000275838.1:p.Pro146=
ENST00000377867.7:c.392_393delinsCT	ENSP00000367098.3:p.Pro131=
ENST00000420175.2:c.437_438delinsCT	ENSP00000391137.2:p.Pro146=
NM_001142459.1:c.437_438delinsCT	NP_001135931.2:p.Pro146=
NM_001142460.1:c.437_438delinsCT	NP_001135932.2:p.Pro146=
NM_080871.3:c.392_393delinsCT	NP_543147.2:p.Pro131=
XM_005249949.3:c.572_573delinsCT	XP_005250006.1:p.Pro191=
NM_001142459.2:c.437_438delinsCT MANE Select	NP_001135931.2:p.Pro146=
NM_080871.4:c.392_393delinsCT	NP_543147.2:p.Pro131=