Canonical Allele Identifier: CA1752544778

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186405_151186406delinsGC , CM000669.2:g.151186405_151186406delinsGC	GRCh38
NC_000007.13:g.150883492_150883493delinsGC , CM000669.1:g.150883492_150883493delinsGC	GRCh37
NC_000007.12:g.150514425_150514426delinsGC	NCBI36
NG_017016.1:g.6427_6428delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.570_571delinsGC MANE Select	ENSP00000391137.2:p.Gly190=
ENST00000275838.5:c.570_571delinsGC	ENSP00000275838.1:p.Gly190=
ENST00000377867.7:c.525_526delinsGC	ENSP00000367098.3:p.Gly175=
ENST00000420175.2:c.570_571delinsGC	ENSP00000391137.2:p.Gly190=
NM_001142459.1:c.570_571delinsGC	NP_001135931.2:p.Gly190=
NM_001142460.1:c.570_571delinsGC	NP_001135932.2:p.Gly190=
NM_080871.3:c.525_526delinsGC	NP_543147.2:p.Gly175=
XM_005249949.3:c.705_706delinsGC	XP_005250006.1:p.Gly235=
NM_001142459.2:c.570_571delinsGC MANE Select	NP_001135931.2:p.Gly190=
NM_080871.4:c.525_526delinsGC	NP_543147.2:p.Gly175=