Canonical Allele Identifier: CA370037356

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150883957A>C (hg19) ; chr7:g.151186870A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186870A>C , CM000669.2:g.151186870A>C	GRCh38
NC_000007.13:g.150883957A>C , CM000669.1:g.150883957A>C	GRCh37
NC_000007.12:g.150514890A>C	NCBI36
NG_017016.1:g.5963T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.261T>G MANE Select	ENSP00000391137.2:p.Phe87Leu
ENST00000275838.5:c.261T>G	ENSP00000275838.1:p.Phe87Leu
ENST00000377867.7:c.272-211T>G	ENSP00000367098.3:n.272-211T>G
ENST00000415615.1:c.*305T>G	ENSP00000410871.1:n.*305T>G
ENST00000420175.2:c.261T>G	ENSP00000391137.2:p.Phe87Leu
NM_001142459.1:c.261T>G	NP_001135931.2:p.Phe87Leu
NM_001142460.1:c.261T>G	NP_001135932.2:p.Phe87Leu
NM_080871.3:c.272-211T>G	NP_543147.2:n.272-211T>G
XM_005249949.3:c.396T>G	XP_005250006.1:p.Phe132Leu
NM_001142459.2:c.261T>G MANE Select	NP_001135931.2:p.Phe87Leu
NM_080871.4:c.272-211T>G	NP_543147.2:n.272-211T>G