Canonical Allele Identifier: CA2710964614
Gene: DSP HGNC NCBI

Linked Data

dbSNP Id: rs2113651225

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7554121_7554122insAA , CM000668.2:g.7554121_7554122insAA GRCh38
NC_000006.11:g.7554354_7554355insAA , CM000668.1:g.7554354_7554355insAA GRCh37
NC_000006.10:g.7499353_7499354insAA NCBI36
NG_008803.1:g.17485_17486insAA , LRG_423:g.17485_17486insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000683682.2:c.171-1597_171-1596insAA ENSP00000508162.2:n.171-1597_171-1596insAA
ENST00000710359.1:c.171-1597_171-1596insAA ENSP00000518230.1:n.171-1597_171-1596insAA
ENST00000683563.1:n.63-1597_63-1596insAA
ENST00000683682.1:c.66-1597_66-1596insAA ENSP00000508162.1:n.66-1597_66-1596insAA
ENST00000379802.8:c.171-1597_171-1596insAA MANE Select ENSP00000369129.3:n.171-1597_171-1596insAA
ENST00000379802.7:c.171-1597_171-1596insAA ENSP00000369129.3:n.171-1597_171-1596insAA
ENST00000418664.2:c.171-1597_171-1596insAA ENSP00000396591.2:n.171-1597_171-1596insAA
NM_001008844.1:c.171-1597_171-1596insAA NP_001008844.1:n.171-1597_171-1596insAA
NM_004415.2:c.171-1597_171-1596insAA , LRG_423t1:c.171-1597_171-1596insAA NP_004406.2:n.171-1597_171-1596insAA
XM_011514323.1:c.171-1597_171-1596insAA XP_011512625.1:n.171-1597_171-1596insAA
NM_001008844.2:c.171-1597_171-1596insAA NP_001008844.1:n.171-1597_171-1596insAA
NM_001319034.1:c.171-1597_171-1596insAA NP_001305963.1:n.171-1597_171-1596insAA
NM_004415.3:c.171-1597_171-1596insAA NP_004406.2:n.171-1597_171-1596insAA
NM_004415.4:c.171-1597_171-1596insAA MANE Select NP_004406.2:n.171-1597_171-1596insAA
NM_001008844.3:c.171-1597_171-1596insAA NP_001008844.1:n.171-1597_171-1596insAA
NM_001319034.2:c.171-1597_171-1596insAA NP_001305963.1:n.171-1597_171-1596insAA