Canonical Allele Identifier: CA2832542908
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7584383_7584384insT , CM000668.2:g.7584383_7584384insT GRCh38
NC_000006.11:g.7584616_7584617insT , CM000668.1:g.7584616_7584617insT GRCh37
NC_000006.10:g.7529615_7529616insT NCBI36
NG_008803.1:g.47747_47748insT , LRG_423:g.47747_47748insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.5792_5793insT ENSP00000518230.1:p.Gly1932ArgfsTer5
ENST00000379802.8:c.7121_7122insT MANE Select ENSP00000369129.3:p.Gly2375ArgfsTer5
ENST00000379802.7:c.7121_7122insT ENSP00000369129.3:p.Gly2375ArgfsTer5
ENST00000418664.2:c.5324_5325insT ENSP00000396591.2:p.Gly1776ArgfsTer5
NM_001008844.1:c.5324_5325insT NP_001008844.1:p.Gly1776ArgfsTer5
NM_004415.2:c.7121_7122insT , LRG_423t1:c.7121_7122insT NP_004406.2:p.Gly2375ArgfsTer5
XM_011514323.1:c.5792_5793insT XP_011512625.1:p.Gly1932ArgfsTer5
NM_001008844.2:c.5324_5325insT NP_001008844.1:p.Gly1776ArgfsTer5
NM_001319034.1:c.5792_5793insT NP_001305963.1:p.Gly1932ArgfsTer5
NM_004415.3:c.7121_7122insT NP_004406.2:p.Gly2375ArgfsTer5
NM_004415.4:c.7121_7122insT MANE Select NP_004406.2:p.Gly2375ArgfsTer5
NM_001008844.3:c.5324_5325insT NP_001008844.1:p.Gly1776ArgfsTer5
NM_001319034.2:c.5792_5793insT NP_001305963.1:p.Gly1932ArgfsTer5