Canonical Allele Identifier: CA370037226

Gene: ASB10

Linked Data

• gnomAD v4: 7-151186844-C-A
• MyVariant Identifiers: chr7:g.150883931C>A (hg19) ; chr7:g.151186844C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186844C>A , CM000669.2:g.151186844C>A	GRCh38
NC_000007.13:g.150883931C>A , CM000669.1:g.150883931C>A	GRCh37
NC_000007.12:g.150514864C>A	NCBI36
NG_017016.1:g.5989G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.287G>T MANE Select	ENSP00000391137.2:p.Arg96Met
ENST00000275838.5:c.287G>T	ENSP00000275838.1:p.Arg96Met
ENST00000377867.7:c.272-185G>T	ENSP00000367098.3:n.272-185G>T
ENST00000415615.1:c.*331G>T	ENSP00000410871.1:n.*331G>T
ENST00000420175.2:c.287G>T	ENSP00000391137.2:p.Arg96Met
NM_001142459.1:c.287G>T	NP_001135931.2:p.Arg96Met
NM_001142460.1:c.287G>T	NP_001135932.2:p.Arg96Met
NM_080871.3:c.272-185G>T	NP_543147.2:n.272-185G>T
XM_005249949.3:c.422G>T	XP_005250006.1:p.Arg141Met
NM_001142459.2:c.287G>T MANE Select	NP_001135931.2:p.Arg96Met
NM_080871.4:c.272-185G>T	NP_543147.2:n.272-185G>T