Canonical Allele Identifier: CA2778433433

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186410dup , CM000669.2:g.151186410dup	GRCh38
NC_000007.13:g.150883497dup , CM000669.1:g.150883497dup	GRCh37
NC_000007.12:g.150514430dup	NCBI36
NG_017016.1:g.6427dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.570dup MANE Select	ENSP00000391137.2:p.Pro191AlafsTer5
ENST00000275838.5:c.570dup	ENSP00000275838.1:p.Pro191AlafsTer5
ENST00000377867.7:c.525dup	ENSP00000367098.3:p.Pro176AlafsTer5
ENST00000420175.2:c.570dup	ENSP00000391137.2:p.Pro191AlafsTer5
NM_001142459.1:c.570dup	NP_001135931.2:p.Pro191AlafsTer5
NM_001142460.1:c.570dup	NP_001135932.2:p.Pro191AlafsTer5
NM_080871.3:c.525dup	NP_543147.2:p.Pro176AlafsTer5
XM_005249949.3:c.705dup	XP_005250006.1:p.Pro236AlafsTer5
NM_001142459.2:c.570dup MANE Select	NP_001135931.2:p.Pro191AlafsTer5
NM_080871.4:c.525dup	NP_543147.2:p.Pro176AlafsTer5