Canonical Allele Identifier: CA370037658

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150884046A>G (hg19) ; chr7:g.151186959A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186959A>G , CM000669.2:g.151186959A>G	GRCh38
NC_000007.13:g.150884046A>G , CM000669.1:g.150884046A>G	GRCh37
NC_000007.12:g.150514979A>G	NCBI36
NG_017016.1:g.5874T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.172T>C MANE Select	ENSP00000391137.2:p.Phe58Leu
ENST00000275838.5:c.172T>C	ENSP00000275838.1:p.Phe58Leu
ENST00000377867.7:c.272-300T>C	ENSP00000367098.3:n.272-300T>C
ENST00000415615.1:c.*216T>C	ENSP00000410871.1:n.*216T>C
ENST00000420175.2:c.172T>C	ENSP00000391137.2:p.Phe58Leu
NM_001142459.1:c.172T>C	NP_001135931.2:p.Phe58Leu
NM_001142460.1:c.172T>C	NP_001135932.2:p.Phe58Leu
NM_080871.3:c.272-300T>C	NP_543147.2:n.272-300T>C
XM_005249949.3:c.307T>C	XP_005250006.1:p.Phe103Leu
NM_001142459.2:c.172T>C MANE Select	NP_001135931.2:p.Phe58Leu
NM_080871.4:c.272-300T>C	NP_543147.2:n.272-300T>C