Canonical Allele Identifier: CA4574030

Gene: ASB10

Linked Data

• dbSNP Id: rs781603263
• ExAC: 7:150884294 A / T
• gnomAD v2: 7-150884294-A-T
• MyVariant Identifiers: chr7:g.150884294A>T (hg19) ; chr7:g.151187207A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187207A>T , CM000669.2:g.151187207A>T	GRCh38
NC_000007.13:g.150884294A>T , CM000669.1:g.150884294A>T	GRCh37
NC_000007.12:g.150515227A>T	NCBI36
NG_017016.1:g.5626T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-77T>A MANE Select	ENSP00000391137.2:n.-77T>A
ENST00000275838.5:c.-77T>A	ENSP00000275838.1:n.-77T>A
ENST00000377867.7:c.271+245T>A	ENSP00000367098.3:n.271+245T>A
ENST00000415615.1:c.*121+47T>A	ENSP00000410871.1:n.*121+47T>A
NM_001142459.1:c.-77T>A	NP_001135931.2:n.-77T>A
NM_001142460.1:c.-77T>A	NP_001135932.2:n.-77T>A
NM_080871.3:c.271+245T>A	NP_543147.2:n.271+245T>A
XM_005249949.3:c.59T>A	XP_005250006.1:p.Phe20Tyr
NM_001142459.2:c.-77T>A MANE Select	NP_001135931.2:n.-77T>A
NM_080871.4:c.271+245T>A	NP_543147.2:n.271+245T>A