Canonical Allele Identifier: CA037429

Gene: DSP

Linked Data

• ClinVar Variation Id: 919542
• ClinVar RCV Id: RCV001177778 ; RCV003769913
• dbSNP Id: rs774512190
• ExAC: 6:7579639 C / T
• gnomAD v2: 6-7579639-C-T
• gnomAD v4: 6-7579406-C-T
• MyVariant Identifiers: chr6:g.7579639C>T (hg19) ; chr6:g.7579406C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7579406C>T , CM000668.2:g.7579406C>T	GRCh38
NC_000006.11:g.7579639C>T , CM000668.1:g.7579639C>T	GRCh37
NC_000006.10:g.7524638C>T	NCBI36
NG_008803.1:g.42770C>T , LRG_423:g.42770C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.3216C>T	ENSP00000518230.1:p.Phe1072=
ENST00000379802.8:c.3216C>T MANE Select	ENSP00000369129.3:p.Phe1072=
ENST00000379802.7:c.3216C>T	ENSP00000369129.3:p.Phe1072=
ENST00000418664.2:c.3216C>T	ENSP00000396591.2:p.Phe1072=
NM_001008844.1:c.3216C>T	NP_001008844.1:p.Phe1072=
NM_004415.2:c.3216C>T , LRG_423t1:c.3216C>T	NP_004406.2:p.Phe1072=
XM_011514323.1:c.3216C>T	XP_011512625.1:p.Phe1072=
NM_001008844.2:c.3216C>T	NP_001008844.1:p.Phe1072=
NM_001319034.1:c.3216C>T	NP_001305963.1:p.Phe1072=
NM_004415.3:c.3216C>T	NP_004406.2:p.Phe1072=
NM_004415.4:c.3216C>T MANE Select	NP_004406.2:p.Phe1072=
NM_001008844.3:c.3216C>T	NP_001008844.1:p.Phe1072=
NM_001319034.2:c.3216C>T	NP_001305963.1:p.Phe1072=