Canonical Allele Identifier: CA2579066552

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186339dup , CM000669.2:g.151186339dup	GRCh38
NC_000007.13:g.150883426dup , CM000669.1:g.150883426dup	GRCh37
NC_000007.12:g.150514359dup	NCBI36
NG_017016.1:g.6495dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.584+54dup MANE Select	ENSP00000391137.2:n.584+54dup
ENST00000275838.5:c.584+54dup	ENSP00000275838.1:n.584+54dup
ENST00000377867.7:c.539+54dup	ENSP00000367098.3:n.539+54dup
ENST00000420175.2:c.584+54dup	ENSP00000391137.2:n.584+54dup
NM_001142459.1:c.584+54dup	NP_001135931.2:n.584+54dup
NM_001142460.1:c.584+54dup	NP_001135932.2:n.584+54dup
NM_080871.3:c.539+54dup	NP_543147.2:n.539+54dup
XM_005249949.3:c.719+54dup	XP_005250006.1:n.719+54dup
NM_001142459.2:c.584+54dup MANE Select	NP_001135931.2:n.584+54dup
NM_080871.4:c.539+54dup	NP_543147.2:n.539+54dup