Canonical Allele Identifier: CA645550293

Gene: ASB10

Linked Data

• COSMIC: COSM5872275 ; COSM5872276 ; COSM5872277

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186905_151186906delinsTT , CM000669.2:g.151186905_151186906delinsTT	GRCh38
NC_000007.13:g.150883992_150883993delinsTT , CM000669.1:g.150883992_150883993delinsTT	GRCh37
NC_000007.12:g.150514925_150514926delinsTT	NCBI36
NG_017016.1:g.5927_5928delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.225_226delinsAA MANE Select	ENSP00000391137.2:p.Asp76Asn
ENST00000275838.5:c.225_226delinsAA	ENSP00000275838.1:p.Asp76Asn
ENST00000377867.7:c.272-247_272-246delinsAA	ENSP00000367098.3:n.272-247_272-246delinsAA
ENST00000415615.1:c.*269_*270delinsAA	ENSP00000410871.1:n.*269_*270delinsAA
ENST00000420175.2:c.225_226delinsAA	ENSP00000391137.2:p.Asp76Asn
NM_001142459.1:c.225_226delinsAA	NP_001135931.2:p.Asp76Asn
NM_001142460.1:c.225_226delinsAA	NP_001135932.2:p.Asp76Asn
NM_080871.3:c.272-247_272-246delinsAA	NP_543147.2:n.272-247_272-246delinsAA
XM_005249949.3:c.360_361delinsAA	XP_005250006.1:p.Asp121Asn
NM_001142459.2:c.225_226delinsAA MANE Select	NP_001135931.2:p.Asp76Asn
NM_080871.4:c.272-247_272-246delinsAA	NP_543147.2:n.272-247_272-246delinsAA