Canonical Allele Identifier: CA052285

Gene: DSP

Linked Data

• ClinVar Variation Id: 3224255
• ClinVar RCV Id: RCV004518981
• dbSNP Id: rs752007344
• ExAC: 6:7585916 C / T
• gnomAD v2: 6-7585916-C-T
• gnomAD v4: 6-7585683-C-T
• COSMIC: COSM3629850
• MyVariant Identifiers: chr6:g.7585916C>T (hg19) ; chr6:g.7585683C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585683C>T , CM000668.2:g.7585683C>T	GRCh38
NC_000006.11:g.7585916C>T , CM000668.1:g.7585916C>T	GRCh37
NC_000006.10:g.7530915C>T	NCBI36
NG_008803.1:g.49047C>T , LRG_423:g.49047C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.7092C>T	ENSP00000518230.1:p.Ser2364=
ENST00000379802.8:c.8421C>T MANE Select	ENSP00000369129.3:p.Ser2807=
ENST00000379802.7:c.8421C>T	ENSP00000369129.3:p.Ser2807=
ENST00000418664.2:c.6624C>T	ENSP00000396591.2:p.Ser2208=
NM_001008844.1:c.6624C>T	NP_001008844.1:p.Ser2208=
NM_004415.2:c.8421C>T , LRG_423t1:c.8421C>T	NP_004406.2:p.Ser2807=
XM_011514323.1:c.7092C>T	XP_011512625.1:p.Ser2364=
NM_001008844.2:c.6624C>T	NP_001008844.1:p.Ser2208=
NM_001319034.1:c.7092C>T	NP_001305963.1:p.Ser2364=
NM_004415.3:c.8421C>T	NP_004406.2:p.Ser2807=
NM_004415.4:c.8421C>T MANE Select	NP_004406.2:p.Ser2807=
NM_001008844.3:c.6624C>T	NP_001008844.1:p.Ser2208=
NM_001319034.2:c.7092C>T	NP_001305963.1:p.Ser2364=