Canonical Allele Identifier: CA2695201875

Gene: ASB10

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187179_151187181delinsCAG , CM000669.2:g.151187179_151187181delinsCAG	GRCh38
NC_000007.13:g.150884266_150884268delinsCAG , CM000669.1:g.150884266_150884268delinsCAG	GRCh37
NC_000007.12:g.150515199_150515201delinsCAG	NCBI36
NG_017016.1:g.5652_5654delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-51_-49delinsCTG MANE Select	ENSP00000391137.2:n.-51_-49delinsCTG
ENST00000275838.5:c.-51_-49delinsCTG	ENSP00000275838.1:n.-51_-49delinsCTG
ENST00000377867.7:c.271+271_271+273delinsCTG	ENSP00000367098.3:n.271+271_271+273delinsCTG
ENST00000415615.1:c.*121+73_*121+75delinsCTG	ENSP00000410871.1:n.*121+73_*121+75delinsCTG
NM_001142459.1:c.-51_-49delinsCTG	NP_001135931.2:n.-51_-49delinsCTG
NM_001142460.1:c.-51_-49delinsCTG	NP_001135932.2:n.-51_-49delinsCTG
NM_080871.3:c.271+271_271+273delinsCTG	NP_543147.2:n.271+271_271+273delinsCTG
XM_005249949.3:c.85_87delinsCTG	XP_005250006.1:p.Leu29=
NM_001142459.2:c.-51_-49delinsCTG MANE Select	NP_001135931.2:n.-51_-49delinsCTG
NM_080871.4:c.271+271_271+273delinsCTG	NP_543147.2:n.271+271_271+273delinsCTG