Canonical Allele Identifier: CA1608623928
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7568995C= , CM000668.2:g.7568995C= GRCh38
NC_000006.11:g.7569228C= , CM000668.1:g.7569228C= GRCh37
NC_000006.10:g.7514227C= NCBI36
NG_008803.1:g.32359C= , LRG_423:g.32359C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.1420-191C= ENSP00000518230.1:n.1420-191C=
ENST00000379802.8:c.1420-191C= MANE Select ENSP00000369129.3:n.1420-191C=
ENST00000379802.7:c.1420-191C= ENSP00000369129.3:n.1420-191C=
ENST00000418664.2:c.1420-191C= ENSP00000396591.2:n.1420-191C=
NM_001008844.1:c.1420-191C= NP_001008844.1:n.1420-191C=
NM_004415.2:c.1420-191C= , LRG_423t1:c.1420-191C= NP_004406.2:n.1420-191C=
XM_011514323.1:c.1420-191C= XP_011512625.1:n.1420-191C=
NM_001008844.2:c.1420-191C= NP_001008844.1:n.1420-191C=
NM_001319034.1:c.1420-191C= NP_001305963.1:n.1420-191C=
NM_004415.3:c.1420-191C= NP_004406.2:n.1420-191C=
NM_004415.4:c.1420-191C= MANE Select NP_004406.2:n.1420-191C=
NM_001008844.3:c.1420-191C= NP_001008844.1:n.1420-191C=
NM_001319034.2:c.1420-191C= NP_001305963.1:n.1420-191C=