Canonical Allele Identifier: CA2579066567

Gene: ASB10

Linked Data

• gnomAD v4: 7-151186794-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186794C>T , CM000669.2:g.151186794C>T	GRCh38
NC_000007.13:g.150883881C>T , CM000669.1:g.150883881C>T	GRCh37
NC_000007.12:g.150514814C>T	NCBI36
NG_017016.1:g.6039G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.316+21G>A MANE Select	ENSP00000391137.2:n.316+21G>A
ENST00000275838.5:c.316+21G>A	ENSP00000275838.1:n.316+21G>A
ENST00000377867.7:c.272-135G>A	ENSP00000367098.3:n.272-135G>A
ENST00000415615.1:c.*360+21G>A	ENSP00000410871.1:n.*360+21G>A
ENST00000420175.2:c.316+21G>A	ENSP00000391137.2:n.316+21G>A
NM_001142459.1:c.316+21G>A	NP_001135931.2:n.316+21G>A
NM_001142460.1:c.316+21G>A	NP_001135932.2:n.316+21G>A
NM_080871.3:c.272-135G>A	NP_543147.2:n.272-135G>A
XM_005249949.3:c.451+21G>A	XP_005250006.1:n.451+21G>A
NM_001142459.2:c.316+21G>A MANE Select	NP_001135931.2:n.316+21G>A
NM_080871.4:c.272-135G>A	NP_543147.2:n.272-135G>A