Canonical Allele Identifier: CA370037678

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150884052G>C (hg19) ; chr7:g.151186965G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186965G>C , CM000669.2:g.151186965G>C	GRCh38
NC_000007.13:g.150884052G>C , CM000669.1:g.150884052G>C	GRCh37
NC_000007.12:g.150514985G>C	NCBI36
NG_017016.1:g.5868C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.166C>G MANE Select	ENSP00000391137.2:p.Leu56Val
ENST00000275838.5:c.166C>G	ENSP00000275838.1:p.Leu56Val
ENST00000377867.7:c.272-306C>G	ENSP00000367098.3:n.272-306C>G
ENST00000415615.1:c.*210C>G	ENSP00000410871.1:n.*210C>G
ENST00000420175.2:c.166C>G	ENSP00000391137.2:p.Leu56Val
NM_001142459.1:c.166C>G	NP_001135931.2:p.Leu56Val
NM_001142460.1:c.166C>G	NP_001135932.2:p.Leu56Val
NM_080871.3:c.272-306C>G	NP_543147.2:n.272-306C>G
XM_005249949.3:c.301C>G	XP_005250006.1:p.Leu101Val
NM_001142459.2:c.166C>G MANE Select	NP_001135931.2:p.Leu56Val
NM_080871.4:c.272-306C>G	NP_543147.2:n.272-306C>G