Canonical Allele Identifier: CA458881722

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150884077G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186990G>T , CM000669.2:g.151186990G>T	GRCh38
NC_000007.13:g.150884077G>T , CM000669.1:g.150884077G>T	GRCh37
NC_000007.12:g.150515010G>T	NCBI36
NG_017016.1:g.5843C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.141C>A MANE Select	ENSP00000391137.2:p.Val47=
ENST00000275838.5:c.141C>A	ENSP00000275838.1:p.Val47=
ENST00000377867.7:c.272-331C>A	ENSP00000367098.3:n.272-331C>A
ENST00000415615.1:c.*185C>A	ENSP00000410871.1:n.*185C>A
ENST00000420175.2:c.141C>A	ENSP00000391137.2:p.Val47=
NM_001142459.1:c.141C>A	NP_001135931.2:p.Val47=
NM_001142460.1:c.141C>A	NP_001135932.2:p.Val47=
NM_080871.3:c.272-331C>A	NP_543147.2:n.272-331C>A
XM_005249949.3:c.276C>A	XP_005250006.1:p.Val92=
NM_001142459.2:c.141C>A MANE Select	NP_001135931.2:p.Val47=
NM_080871.4:c.272-331C>A	NP_543147.2:n.272-331C>A