Canonical Allele Identifier: CA034109

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7555806C>G , CM000668.2:g.7555806C>G	GRCh38
NC_000006.11:g.7556039C>G , CM000668.1:g.7556039C>G	GRCh37
NC_000006.10:g.7501038C>G	NCBI36
NG_008803.1:g.19170C>G , LRG_423:g.19170C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004415.4:c.259C>G MANE Select	NP_004406.2:p.Leu87Val
ENST00000379802.8:c.259C>G MANE Select	ENSP00000369129.3:p.Leu87Val
NM_001008844.1:c.259C>G	NP_001008844.1:p.Leu87Val
NM_001008844.2:c.259C>G	NP_001008844.1:p.Leu87Val
NM_001008844.3:c.259C>G	NP_001008844.1:p.Leu87Val
NM_001319034.1:c.259C>G	NP_001305963.1:p.Leu87Val
NM_001319034.2:c.259C>G	NP_001305963.1:p.Leu87Val
NM_004415.2:c.259C>G , LRG_423t1:c.259C>G	NP_004406.2:p.Leu87Val
NM_004415.3:c.259C>G	NP_004406.2:p.Leu87Val
ENST00000379802.7:c.259C>G	ENSP00000369129.3:p.Leu87Val
ENST00000418664.2:c.259C>G	ENSP00000396591.2:p.Leu87Val
ENST00000683563.1:n.151C>G
ENST00000683682.1:c.154C>G	ENSP00000508162.1:p.Leu52Val
ENST00000683682.2:c.259C>G	ENSP00000508162.2:p.Leu87Val
ENST00000710359.1:c.259C>G	ENSP00000518230.1:p.Leu87Val
XM_011514323.1:c.259C>G	XP_011512625.1:p.Leu87Val