Canonical Allele Identifier: CA652038832

Gene: ASB10

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186674_151186675insT , CM000669.2:g.151186674_151186675insT	GRCh38
NC_000007.13:g.150883761_150883762insT , CM000669.1:g.150883761_150883762insT	GRCh37
NC_000007.12:g.150514694_150514695insT	NCBI36
NG_017016.1:g.6158_6159insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.317-16_317-15insA MANE Select	ENSP00000391137.2:n.317-16_317-15insA
ENST00000275838.5:c.317-16_317-15insA	ENSP00000275838.1:n.317-16_317-15insA
ENST00000377867.7:c.272-16_272-15insA	ENSP00000367098.3:n.272-16_272-15insA
ENST00000415615.1:c.*361-16_*361-15insA	ENSP00000410871.1:n.*361-16_*361-15insA
ENST00000420175.2:c.317-16_317-15insA	ENSP00000391137.2:n.317-16_317-15insA
NM_001142459.1:c.317-16_317-15insA	NP_001135931.2:n.317-16_317-15insA
NM_001142460.1:c.317-16_317-15insA	NP_001135932.2:n.317-16_317-15insA
NM_080871.3:c.272-16_272-15insA	NP_543147.2:n.272-16_272-15insA
XM_005249949.3:c.452-16_452-15insA	XP_005250006.1:n.452-16_452-15insA
NM_001142459.2:c.317-16_317-15insA MANE Select	NP_001135931.2:n.317-16_317-15insA
NM_080871.4:c.272-16_272-15insA	NP_543147.2:n.272-16_272-15insA