Canonical Allele Identifier: CA1752546085

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187209_151187213delinsTACAG , CM000669.2:g.151187209_151187213delinsTACAG	GRCh38
NC_000007.13:g.150884296_150884300delinsTACAG , CM000669.1:g.150884296_150884300delinsTACAG	GRCh37
NC_000007.12:g.150515229_150515233delinsTACAG	NCBI36
NG_017016.1:g.5620_5624delinsCTGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-83_-79delinsCTGTA MANE Select	ENSP00000391137.2:n.-83_-79delinsCTGTA
ENST00000275838.5:c.-83_-79delinsCTGTA	ENSP00000275838.1:n.-83_-79delinsCTGTA
ENST00000377867.7:c.271+239_271+243delinsCTGTA	ENSP00000367098.3:n.271+239_271+243delinsCTGTA
ENST00000415615.1:c.*121+41_*121+45delinsCTGTA	ENSP00000410871.1:n.*121+41_*121+45delinsCTGTA
NM_001142459.1:c.-83_-79delinsCTGTA	NP_001135931.2:n.-83_-79delinsCTGTA
NM_001142460.1:c.-83_-79delinsCTGTA	NP_001135932.2:n.-83_-79delinsCTGTA
NM_080871.3:c.271+239_271+243delinsCTGTA	NP_543147.2:n.271+239_271+243delinsCTGTA
XM_005249949.3:c.53_57delinsCTGTA	XP_005250006.1:p.Ser18=
NM_001142459.2:c.-83_-79delinsCTGTA MANE Select	NP_001135931.2:n.-83_-79delinsCTGTA
NM_080871.4:c.271+239_271+243delinsCTGTA	NP_543147.2:n.271+239_271+243delinsCTGTA