Canonical Allele Identifier: CA049027

Gene: DSP

Linked Data

• dbSNP Id: rs748356667
• ExAC: 6:7584536 C / G
• gnomAD v2: 6-7584536-C-G
• gnomAD v3: 6-7584303-C-G
• gnomAD v4: 6-7584303-C-G
• MyVariant Identifiers: chr6:g.7584536C>G (hg19) ; chr6:g.7584303C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7584303C>G , CM000668.2:g.7584303C>G	GRCh38
NC_000006.11:g.7584536C>G , CM000668.1:g.7584536C>G	GRCh37
NC_000006.10:g.7529535C>G	NCBI36
NG_008803.1:g.47667C>G , LRG_423:g.47667C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.5712C>G	ENSP00000518230.1:p.Ile1904Met
ENST00000379802.8:c.7041C>G MANE Select	ENSP00000369129.3:p.Ile2347Met
ENST00000379802.7:c.7041C>G	ENSP00000369129.3:p.Ile2347Met
ENST00000418664.2:c.5244C>G	ENSP00000396591.2:p.Ile1748Met
NM_001008844.1:c.5244C>G	NP_001008844.1:p.Ile1748Met
NM_004415.2:c.7041C>G , LRG_423t1:c.7041C>G	NP_004406.2:p.Ile2347Met
XM_011514323.1:c.5712C>G	XP_011512625.1:p.Ile1904Met
NM_001008844.2:c.5244C>G	NP_001008844.1:p.Ile1748Met
NM_001319034.1:c.5712C>G	NP_001305963.1:p.Ile1904Met
NM_004415.3:c.7041C>G	NP_004406.2:p.Ile2347Met
NM_004415.4:c.7041C>G MANE Select	NP_004406.2:p.Ile2347Met
NM_001008844.3:c.5244C>G	NP_001008844.1:p.Ile1748Met
NM_001319034.2:c.5712C>G	NP_001305963.1:p.Ile1904Met