Canonical Allele Identifier: CA169125877

Gene: ASB10

Linked Data

• dbSNP Id: rs1024644696
• MyVariant Identifiers: chr7:g.150884013_150884014insGG (hg19) ; chr7:g.151186926_151186927insGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186927_151186928insGG , CM000669.2:g.151186927_151186928insGG	GRCh38
NC_000007.13:g.150884014_150884015insGG , CM000669.1:g.150884014_150884015insGG	GRCh37
NC_000007.12:g.150514947_150514948insGG	NCBI36
NG_017016.1:g.5906_5907insCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000420175.3:c.204_205insCC MANE Select	ENSP00000391137.2:p.Cys69ProfsTer?
ENST00000275838.5:c.204_205insCC	ENSP00000275838.1:p.Cys69ProfsTer?
ENST00000377867.7:c.272-268_272-267insCC	ENSP00000367098.3:n.272-268_272-267insCC
ENST00000415615.1:c.*248_*249insCC	ENSP00000410871.1:n.*248_*249insCC
ENST00000420175.2:c.204_205insCC	ENSP00000391137.2:p.Cys69ProfsTer?
NM_001142459.1:c.204_205insCC	NP_001135931.2:p.Cys69ProfsTer?
NM_001142460.1:c.204_205insCC	NP_001135932.2:p.Cys69ProfsTer?
NM_080871.3:c.272-268_272-267insCC	NP_543147.2:n.272-268_272-267insCC
XM_005249949.3:c.339_340insCC	XP_005250006.1:p.Cys114ProfsTer?
NM_001142459.2:c.204_205insCC MANE Select	NP_001135931.2:p.Cys69ProfsTer?
NM_080871.4:c.272-268_272-267insCC	NP_543147.2:n.272-268_272-267insCC