Canonical Allele Identifier: CA133973976

Gene: DSP

Linked Data

• ClinVar Variation Id: 1332270
• ClinVar RCV Id: RCV001805316 ; RCV002542395 ; RCV004009119
• dbSNP Id: rs376397314
• gnomAD v4: 6-7583180-A-G
• MyVariant Identifiers: chr6:g.7583413A>G (hg19) ; chr6:g.7583180A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583180A>G , CM000668.2:g.7583180A>G	GRCh38
NC_000006.11:g.7583413A>G , CM000668.1:g.7583413A>G	GRCh37
NC_000006.10:g.7528412A>G	NCBI36
NG_008803.1:g.46544A>G , LRG_423:g.46544A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4589A>G	ENSP00000518230.1:p.Lys1530Arg
ENST00000379802.8:c.5918A>G MANE Select	ENSP00000369129.3:p.Lys1973Arg
ENST00000379802.7:c.5918A>G	ENSP00000369129.3:p.Lys1973Arg
ENST00000418664.2:c.4121A>G	ENSP00000396591.2:p.Lys1374Arg
NM_001008844.1:c.4121A>G	NP_001008844.1:p.Lys1374Arg
NM_004415.2:c.5918A>G , LRG_423t1:c.5918A>G	NP_004406.2:p.Lys1973Arg
XM_011514323.1:c.4589A>G	XP_011512625.1:p.Lys1530Arg
NM_001008844.2:c.4121A>G	NP_001008844.1:p.Lys1374Arg
NM_001319034.1:c.4589A>G	NP_001305963.1:p.Lys1530Arg
NM_004415.3:c.5918A>G	NP_004406.2:p.Lys1973Arg
NM_004415.4:c.5918A>G MANE Select	NP_004406.2:p.Lys1973Arg
NM_001008844.3:c.4121A>G	NP_001008844.1:p.Lys1374Arg
NM_001319034.2:c.4589A>G	NP_001305963.1:p.Lys1530Arg