Canonical Allele Identifier: CA448716971

Gene: DSP

Linked Data

• ClinVar Variation Id: 2775370
• ClinVar RCV Id: RCV003533780 ; RCV004011643
• gnomAD v4: 6-7585197-C-T
• MyVariant Identifiers: chr6:g.7585430C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585197C>T , CM000668.2:g.7585197C>T	GRCh38
NC_000006.11:g.7585430C>T , CM000668.1:g.7585430C>T	GRCh37
NC_000006.10:g.7530429C>T	NCBI36
NG_008803.1:g.48561C>T , LRG_423:g.48561C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6606C>T	ENSP00000518230.1:p.Ile2202=
ENST00000379802.8:c.7935C>T MANE Select	ENSP00000369129.3:p.Ile2645=
ENST00000379802.7:c.7935C>T	ENSP00000369129.3:p.Ile2645=
ENST00000418664.2:c.6138C>T	ENSP00000396591.2:p.Ile2046=
NM_001008844.1:c.6138C>T	NP_001008844.1:p.Ile2046=
NM_004415.2:c.7935C>T , LRG_423t1:c.7935C>T	NP_004406.2:p.Ile2645=
XM_011514323.1:c.6606C>T	XP_011512625.1:p.Ile2202=
NM_001008844.2:c.6138C>T	NP_001008844.1:p.Ile2046=
NM_001319034.1:c.6606C>T	NP_001305963.1:p.Ile2202=
NM_004415.3:c.7935C>T	NP_004406.2:p.Ile2645=
NM_004415.4:c.7935C>T MANE Select	NP_004406.2:p.Ile2645=
NM_001008844.3:c.6138C>T	NP_001008844.1:p.Ile2046=
NM_001319034.2:c.6606C>T	NP_001305963.1:p.Ile2202=