Canonical Allele Identifier: CA1752544724

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186370_151186371delinsGT , CM000669.2:g.151186370_151186371delinsGT	GRCh38
NC_000007.13:g.150883457_150883458delinsGT , CM000669.1:g.150883457_150883458delinsGT	GRCh37
NC_000007.12:g.150514390_150514391delinsGT	NCBI36
NG_017016.1:g.6462_6463delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.584+21_584+22delinsAC MANE Select	ENSP00000391137.2:n.584+21_584+22delinsAC
ENST00000275838.5:c.584+21_584+22delinsAC	ENSP00000275838.1:n.584+21_584+22delinsAC
ENST00000377867.7:c.539+21_539+22delinsAC	ENSP00000367098.3:n.539+21_539+22delinsAC
ENST00000420175.2:c.584+21_584+22delinsAC	ENSP00000391137.2:n.584+21_584+22delinsAC
NM_001142459.1:c.584+21_584+22delinsAC	NP_001135931.2:n.584+21_584+22delinsAC
NM_001142460.1:c.584+21_584+22delinsAC	NP_001135932.2:n.584+21_584+22delinsAC
NM_080871.3:c.539+21_539+22delinsAC	NP_543147.2:n.539+21_539+22delinsAC
XM_005249949.3:c.719+21_719+22delinsAC	XP_005250006.1:n.719+21_719+22delinsAC
NM_001142459.2:c.584+21_584+22delinsAC MANE Select	NP_001135931.2:n.584+21_584+22delinsAC
NM_080871.4:c.539+21_539+22delinsAC	NP_543147.2:n.539+21_539+22delinsAC