Canonical Allele Identifier: CA448715729

Gene: DSP

Linked Data

• COSMIC: COSM1445909
• MyVariant Identifiers: chr6:g.7583582C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583349C>T , CM000668.2:g.7583349C>T	GRCh38
NC_000006.11:g.7583582C>T , CM000668.1:g.7583582C>T	GRCh37
NC_000006.10:g.7528581C>T	NCBI36
NG_008803.1:g.46713C>T , LRG_423:g.46713C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4758C>T	ENSP00000518230.1:p.Tyr1586=
ENST00000379802.8:c.6087C>T MANE Select	ENSP00000369129.3:p.Tyr2029=
ENST00000379802.7:c.6087C>T	ENSP00000369129.3:p.Tyr2029=
ENST00000418664.2:c.4290C>T	ENSP00000396591.2:p.Tyr1430=
NM_001008844.1:c.4290C>T	NP_001008844.1:p.Tyr1430=
NM_004415.2:c.6087C>T , LRG_423t1:c.6087C>T	NP_004406.2:p.Tyr2029=
XM_011514323.1:c.4758C>T	XP_011512625.1:p.Tyr1586=
NM_001008844.2:c.4290C>T	NP_001008844.1:p.Tyr1430=
NM_001319034.1:c.4758C>T	NP_001305963.1:p.Tyr1586=
NM_004415.3:c.6087C>T	NP_004406.2:p.Tyr2029=
NM_004415.4:c.6087C>T MANE Select	NP_004406.2:p.Tyr2029=
NM_001008844.3:c.4290C>T	NP_001008844.1:p.Tyr1430=
NM_001319034.2:c.4758C>T	NP_001305963.1:p.Tyr1586=