Canonical Allele Identifier: CA2677232953

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7541588_7541643del , CM000668.2:g.7541588_7541643del GRCh38
NC_000006.11:g.7541821_7541876del , CM000668.1:g.7541821_7541876del GRCh37
NC_000006.10:g.7486820_7486875del NCBI36
NG_008803.1:g.4952_5007del , LRG_423:g.4952_5007del

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.-328_-273del (DSP) ENSP00000518230.1:n.-328_-273del
ENST00000379802.7:c.-328_-273del (DSP) ENSP00000369129.3:n.-328_-273del
XM_011514323.1:c.-328_-273del (DSP) XP_011512625.1:n.-328_-273del
XR_241971.2:n.269-587_269-532del (DSP-AS1)
NM_001008844.2:c.-328_-273del (DSP) NP_001008844.1:n.-328_-273del
NM_001319034.1:c.-328_-273del (DSP) NP_001305963.1:n.-328_-273del
NM_004415.3:c.-328_-273del (DSP) NP_004406.2:n.-328_-273del
XR_241970.4:n.87_142del (DSP-AS1)
XR_241971.3:n.270-587_270-532del (DSP-AS1)