Canonical Allele Identifier: CA458881269

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150883481A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186394A>G , CM000669.2:g.151186394A>G	GRCh38
NC_000007.13:g.150883481A>G , CM000669.1:g.150883481A>G	GRCh37
NC_000007.12:g.150514414A>G	NCBI36
NG_017016.1:g.6439T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.582T>C MANE Select	ENSP00000391137.2:p.Leu194=
ENST00000275838.5:c.582T>C	ENSP00000275838.1:p.Leu194=
ENST00000377867.7:c.537T>C	ENSP00000367098.3:p.Leu179=
ENST00000420175.2:c.582T>C	ENSP00000391137.2:p.Leu194=
NM_001142459.1:c.582T>C	NP_001135931.2:p.Leu194=
NM_001142460.1:c.582T>C	NP_001135932.2:p.Leu194=
NM_080871.3:c.537T>C	NP_543147.2:p.Leu179=
XM_005249949.3:c.717T>C	XP_005250006.1:p.Leu239=
NM_001142459.2:c.582T>C MANE Select	NP_001135931.2:p.Leu194=
NM_080871.4:c.537T>C	NP_543147.2:p.Leu179=