Canonical Allele Identifier: CA448715492

Gene: DSP

Linked Data

• ClinVar Variation Id: 3071205
• ClinVar RCV Id: RCV004014707
• dbSNP Id: rs879254349
• gnomAD v2: 6-7583201-C-T
• gnomAD v3: 6-7582968-C-T
• gnomAD v4: 6-7582968-C-T
• MyVariant Identifiers: chr6:g.7583201C>T (hg19) ; chr6:g.7582968C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7582968C>T , CM000668.2:g.7582968C>T	GRCh38
NC_000006.11:g.7583201C>T , CM000668.1:g.7583201C>T	GRCh37
NC_000006.10:g.7528200C>T	NCBI36
NG_008803.1:g.46332C>T , LRG_423:g.46332C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4377C>T	ENSP00000518230.1:p.Leu1459=
ENST00000379802.8:c.5706C>T MANE Select	ENSP00000369129.3:p.Leu1902=
ENST00000379802.7:c.5706C>T	ENSP00000369129.3:p.Leu1902=
ENST00000418664.2:c.3909C>T	ENSP00000396591.2:p.Leu1303=
NM_001008844.1:c.3909C>T	NP_001008844.1:p.Leu1303=
NM_004415.2:c.5706C>T , LRG_423t1:c.5706C>T	NP_004406.2:p.Leu1902=
XM_011514323.1:c.4377C>T	XP_011512625.1:p.Leu1459=
NM_001008844.2:c.3909C>T	NP_001008844.1:p.Leu1303=
NM_001319034.1:c.4377C>T	NP_001305963.1:p.Leu1459=
NM_004415.3:c.5706C>T	NP_004406.2:p.Leu1902=
NM_004415.4:c.5706C>T MANE Select	NP_004406.2:p.Leu1902=
NM_001008844.3:c.3909C>T	NP_001008844.1:p.Leu1303=
NM_001319034.2:c.4377C>T	NP_001305963.1:p.Leu1459=