Canonical Allele Identifier: CA2685657514

Gene: ASB10

Linked Data

• gnomAD v4: 7-151186422-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186427dup , CM000669.2:g.151186427dup	GRCh38
NC_000007.13:g.150883514dup , CM000669.1:g.150883514dup	GRCh37
NC_000007.12:g.150514447dup	NCBI36
NG_017016.1:g.6410dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.553dup MANE Select	ENSP00000391137.2:p.Leu185ProfsTer11
ENST00000275838.5:c.553dup	ENSP00000275838.1:p.Leu185ProfsTer11
ENST00000377867.7:c.508dup	ENSP00000367098.3:p.Leu170ProfsTer11
ENST00000420175.2:c.553dup	ENSP00000391137.2:p.Leu185ProfsTer11
NM_001142459.1:c.553dup	NP_001135931.2:p.Leu185ProfsTer11
NM_001142460.1:c.553dup	NP_001135932.2:p.Leu185ProfsTer11
NM_080871.3:c.508dup	NP_543147.2:p.Leu170ProfsTer11
XM_005249949.3:c.688dup	XP_005250006.1:p.Leu230ProfsTer11
NM_001142459.2:c.553dup MANE Select	NP_001135931.2:p.Leu185ProfsTer11
NM_080871.4:c.508dup	NP_543147.2:p.Leu170ProfsTer11