Canonical Allele Identifier: CA4573848

Gene: ASB10

Linked Data

• dbSNP Id: rs781133941
• ExAC: 7:150883459 T / A
• gnomAD v2: 7-150883459-T-A
• gnomAD v4: 7-151186372-T-A
• MyVariant Identifiers: chr7:g.150883459T>A (hg19) ; chr7:g.151186372T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186372T>A , CM000669.2:g.151186372T>A	GRCh38
NC_000007.13:g.150883459T>A , CM000669.1:g.150883459T>A	GRCh37
NC_000007.12:g.150514392T>A	NCBI36
NG_017016.1:g.6461A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000420175.3:c.584+20A>T MANE Select	ENSP00000391137.2:n.584+20A>T
ENST00000275838.5:c.584+20A>T	ENSP00000275838.1:n.584+20A>T
ENST00000377867.7:c.539+20A>T	ENSP00000367098.3:n.539+20A>T
ENST00000420175.2:c.584+20A>T	ENSP00000391137.2:n.584+20A>T
NM_001142459.1:c.584+20A>T	NP_001135931.2:n.584+20A>T
NM_001142460.1:c.584+20A>T	NP_001135932.2:n.584+20A>T
NM_080871.3:c.539+20A>T	NP_543147.2:n.539+20A>T
XM_005249949.3:c.719+20A>T	XP_005250006.1:n.719+20A>T
NM_001142459.2:c.584+20A>T MANE Select	NP_001135931.2:n.584+20A>T
NM_080871.4:c.539+20A>T	NP_543147.2:n.539+20A>T