Canonical Allele Identifier: CA169126337

Gene: ASB10

Linked Data

• dbSNP Id: rs148358766
• MyVariant Identifiers: chr7:g.150884276_150884277insGA (hg19) ; chr7:g.151187189_151187190insGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187189_151187190insGA , CM000669.2:g.151187189_151187190insGA	GRCh38
NC_000007.13:g.150884276_150884277insGA , CM000669.1:g.150884276_150884277insGA	GRCh37
NC_000007.12:g.150515209_150515210insGA	NCBI36
NG_017016.1:g.5643_5644insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-60_-59insTC MANE Select	ENSP00000391137.2:n.-60_-59insTC
ENST00000275838.5:c.-60_-59insTC	ENSP00000275838.1:n.-60_-59insTC
ENST00000377867.7:c.271+262_271+263insTC	ENSP00000367098.3:n.271+262_271+263insTC
ENST00000415615.1:c.*121+64_*121+65insTC	ENSP00000410871.1:n.*121+64_*121+65insTC
NM_001142459.1:c.-60_-59insTC	NP_001135931.2:n.-60_-59insTC
NM_001142460.1:c.-60_-59insTC	NP_001135932.2:n.-60_-59insTC
NM_080871.3:c.271+262_271+263insTC	NP_543147.2:n.271+262_271+263insTC
XM_005249949.3:c.76_77insTC	XP_005250006.1:p.Ser26PhefsTer24
NM_001142459.2:c.-60_-59insTC MANE Select	NP_001135931.2:n.-60_-59insTC
NM_080871.4:c.271+262_271+263insTC	NP_543147.2:n.271+262_271+263insTC