Canonical Allele Identifier: CA1608622877
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7568456T= , CM000668.2:g.7568456T= GRCh38
NC_000006.11:g.7568689T= , CM000668.1:g.7568689T= GRCh37
NC_000006.10:g.7513688T= NCBI36
NG_008803.1:g.31820T= , LRG_423:g.31820T=

Transcript Alleles

HGVS Amino-acid change
ENST00000710359.1:c.1286T= ENSP00000518230.1:p.Leu429=
ENST00000682228.1:n.1471T=
ENST00000379802.8:c.1286T= MANE Select ENSP00000369129.3:p.Leu429=
ENST00000379802.7:c.1286T= ENSP00000369129.3:p.Leu429=
ENST00000418664.2:c.1286T= ENSP00000396591.2:p.Leu429=
NM_001008844.1:c.1286T= NP_001008844.1:p.Leu429=
NM_004415.2:c.1286T= , LRG_423t1:c.1286T= NP_004406.2:p.Leu429=
XM_011514323.1:c.1286T= XP_011512625.1:p.Leu429=
NM_001008844.2:c.1286T= NP_001008844.1:p.Leu429=
NM_001319034.1:c.1286T= NP_001305963.1:p.Leu429=
NM_004415.3:c.1286T= NP_004406.2:p.Leu429=
NM_004415.4:c.1286T= MANE Select NP_004406.2:p.Leu429=
NM_001008844.3:c.1286T= NP_001008844.1:p.Leu429=
NM_001319034.2:c.1286T= NP_001305963.1:p.Leu429=