Canonical Allele Identifier: CA2685657567

Gene: ASB10

Linked Data

• gnomAD v4: 7-151186729-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186729G>T , CM000669.2:g.151186729G>T	GRCh38
NC_000007.13:g.150883816G>T , CM000669.1:g.150883816G>T	GRCh37
NC_000007.12:g.150514749G>T	NCBI36
NG_017016.1:g.6104C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.317-70C>A MANE Select	ENSP00000391137.2:n.317-70C>A
ENST00000275838.5:c.317-70C>A	ENSP00000275838.1:n.317-70C>A
ENST00000377867.7:c.272-70C>A	ENSP00000367098.3:n.272-70C>A
ENST00000415615.1:c.*361-70C>A	ENSP00000410871.1:n.*361-70C>A
ENST00000420175.2:c.317-70C>A	ENSP00000391137.2:n.317-70C>A
NM_001142459.1:c.317-70C>A	NP_001135931.2:n.317-70C>A
NM_001142460.1:c.317-70C>A	NP_001135932.2:n.317-70C>A
NM_080871.3:c.272-70C>A	NP_543147.2:n.272-70C>A
XM_005249949.3:c.452-70C>A	XP_005250006.1:n.452-70C>A
NM_001142459.2:c.317-70C>A MANE Select	NP_001135931.2:n.317-70C>A
NM_080871.4:c.272-70C>A	NP_543147.2:n.272-70C>A