Canonical Allele Identifier: CA579077198

Gene: ASB10

Linked Data

• dbSNP Id: rs1412376079
• gnomAD v2: 7-150883428-C-CT
• gnomAD v4: 7-151186341-C-CT
• MyVariant Identifiers: chr7:g.150883428_150883429insT (hg19) ; chr7:g.151186341_151186342insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186344dup , CM000669.2:g.151186344dup	GRCh38
NC_000007.13:g.150883431dup , CM000669.1:g.150883431dup	GRCh37
NC_000007.12:g.150514364dup	NCBI36
NG_017016.1:g.6491dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.584+50dup MANE Select	ENSP00000391137.2:n.584+50dup
ENST00000275838.5:c.584+50dup	ENSP00000275838.1:n.584+50dup
ENST00000377867.7:c.539+50dup	ENSP00000367098.3:n.539+50dup
ENST00000420175.2:c.584+50dup	ENSP00000391137.2:n.584+50dup
NM_001142459.1:c.584+50dup	NP_001135931.2:n.584+50dup
NM_001142460.1:c.584+50dup	NP_001135932.2:n.584+50dup
NM_080871.3:c.539+50dup	NP_543147.2:n.539+50dup
XM_005249949.3:c.719+50dup	XP_005250006.1:n.719+50dup
NM_001142459.2:c.584+50dup MANE Select	NP_001135931.2:n.584+50dup
NM_080871.4:c.539+50dup	NP_543147.2:n.539+50dup