Canonical Allele Identifier: CA4573942

Gene: ASB10

Linked Data

• dbSNP Id: rs762325242
• ExAC: 7:150883898 G / A
• gnomAD v2: 7-150883898-G-A
• gnomAD v3: 7-151186811-G-A
• gnomAD v4: 7-151186811-G-A
• COSMIC: COSM5091431 ; COSM5091432 ; COSM5091433
• MyVariant Identifiers: chr7:g.150883898G>A (hg19) ; chr7:g.151186811G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186811G>A , CM000669.2:g.151186811G>A	GRCh38
NC_000007.13:g.150883898G>A , CM000669.1:g.150883898G>A	GRCh37
NC_000007.12:g.150514831G>A	NCBI36
NG_017016.1:g.6022C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.316+4C>T MANE Select	ENSP00000391137.2:n.316+4C>T
ENST00000275838.5:c.316+4C>T	ENSP00000275838.1:n.316+4C>T
ENST00000377867.7:c.272-152C>T	ENSP00000367098.3:n.272-152C>T
ENST00000415615.1:c.*360+4C>T	ENSP00000410871.1:n.*360+4C>T
ENST00000420175.2:c.316+4C>T	ENSP00000391137.2:n.316+4C>T
NM_001142459.1:c.316+4C>T	NP_001135931.2:n.316+4C>T
NM_001142460.1:c.316+4C>T	NP_001135932.2:n.316+4C>T
NM_080871.3:c.272-152C>T	NP_543147.2:n.272-152C>T
XM_005249949.3:c.451+4C>T	XP_005250006.1:n.451+4C>T
NM_001142459.2:c.316+4C>T MANE Select	NP_001135931.2:n.316+4C>T
NM_080871.4:c.272-152C>T	NP_543147.2:n.272-152C>T