Canonical Allele Identifier: CA362689604

Gene: DSP

Linked Data

• MyVariant Identifiers: chr6:g.7583370T>G (hg19) ; chr6:g.7583137T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583137T>G , CM000668.2:g.7583137T>G	GRCh38
NC_000006.11:g.7583370T>G , CM000668.1:g.7583370T>G	GRCh37
NC_000006.10:g.7528369T>G	NCBI36
NG_008803.1:g.46501T>G , LRG_423:g.46501T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4546T>G	ENSP00000518230.1:p.Trp1516Gly
ENST00000379802.8:c.5875T>G MANE Select	ENSP00000369129.3:p.Trp1959Gly
ENST00000379802.7:c.5875T>G	ENSP00000369129.3:p.Trp1959Gly
ENST00000418664.2:c.4078T>G	ENSP00000396591.2:p.Trp1360Gly
NM_001008844.1:c.4078T>G	NP_001008844.1:p.Trp1360Gly
NM_004415.2:c.5875T>G , LRG_423t1:c.5875T>G	NP_004406.2:p.Trp1959Gly
XM_011514323.1:c.4546T>G	XP_011512625.1:p.Trp1516Gly
NM_001008844.2:c.4078T>G	NP_001008844.1:p.Trp1360Gly
NM_001319034.1:c.4546T>G	NP_001305963.1:p.Trp1516Gly
NM_004415.3:c.5875T>G	NP_004406.2:p.Trp1959Gly
NM_004415.4:c.5875T>G MANE Select	NP_004406.2:p.Trp1959Gly
NM_001008844.3:c.4078T>G	NP_001008844.1:p.Trp1360Gly
NM_001319034.2:c.4546T>G	NP_001305963.1:p.Trp1516Gly