Canonical Allele Identifier: CA2769905078
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7565736_7565737insACCCAA , CM000668.2:g.7565736_7565737insACCCAA GRCh38
NC_000006.11:g.7565969_7565970insACCCAA , CM000668.1:g.7565969_7565970insACCCAA GRCh37
NC_000006.10:g.7510968_7510969insACCCAA NCBI36
NG_008803.1:g.29100_29101insACCCAA , LRG_423:g.29100_29101insACCCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.939+216_939+217insACCCAA ENSP00000518230.1:n.939+216_939+217insACCCAA
ENST00000682228.1:n.263+216_263+217insACCCAA
ENST00000379802.8:c.939+216_939+217insACCCAA MANE Select ENSP00000369129.3:n.939+216_939+217insACCCAA
ENST00000379802.7:c.939+216_939+217insACCCAA ENSP00000369129.3:n.939+216_939+217insACCCAA
ENST00000418664.2:c.939+216_939+217insACCCAA ENSP00000396591.2:n.939+216_939+217insACCCAA
ENST00000506617.1:n.673_674insACCCAA
NM_001008844.1:c.939+216_939+217insACCCAA NP_001008844.1:n.939+216_939+217insACCCAA
NM_004415.2:c.939+216_939+217insACCCAA , LRG_423t1:c.939+216_939+217insACCCAA NP_004406.2:n.939+216_939+217insACCCAA
XM_011514323.1:c.939+216_939+217insACCCAA XP_011512625.1:n.939+216_939+217insACCCAA
NM_001008844.2:c.939+216_939+217insACCCAA NP_001008844.1:n.939+216_939+217insACCCAA
NM_001319034.1:c.939+216_939+217insACCCAA NP_001305963.1:n.939+216_939+217insACCCAA
NM_004415.3:c.939+216_939+217insACCCAA NP_004406.2:n.939+216_939+217insACCCAA
NM_004415.4:c.939+216_939+217insACCCAA MANE Select NP_004406.2:n.939+216_939+217insACCCAA
NM_001008844.3:c.939+216_939+217insACCCAA NP_001008844.1:n.939+216_939+217insACCCAA
NM_001319034.2:c.939+216_939+217insACCCAA NP_001305963.1:n.939+216_939+217insACCCAA