Canonical Allele Identifier: CA370037342

Gene: ASB10

Linked Data

• gnomAD v4: 7-151186866-T-C
• COSMIC: COSM3879413 ; COSM3879414 ; COSM3879415
• MyVariant Identifiers: chr7:g.150883953T>C (hg19) ; chr7:g.151186866T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186866T>C , CM000669.2:g.151186866T>C	GRCh38
NC_000007.13:g.150883953T>C , CM000669.1:g.150883953T>C	GRCh37
NC_000007.12:g.150514886T>C	NCBI36
NG_017016.1:g.5967A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.265A>G MANE Select	ENSP00000391137.2:p.Thr89Ala
ENST00000275838.5:c.265A>G	ENSP00000275838.1:p.Thr89Ala
ENST00000377867.7:c.272-207A>G	ENSP00000367098.3:n.272-207A>G
ENST00000415615.1:c.*309A>G	ENSP00000410871.1:n.*309A>G
ENST00000420175.2:c.265A>G	ENSP00000391137.2:p.Thr89Ala
NM_001142459.1:c.265A>G	NP_001135931.2:p.Thr89Ala
NM_001142460.1:c.265A>G	NP_001135932.2:p.Thr89Ala
NM_080871.3:c.272-207A>G	NP_543147.2:n.272-207A>G
XM_005249949.3:c.400A>G	XP_005250006.1:p.Thr134Ala
NM_001142459.2:c.265A>G MANE Select	NP_001135931.2:p.Thr89Ala
NM_080871.4:c.272-207A>G	NP_543147.2:n.272-207A>G