Canonical Allele Identifier: CA448527300

Gene: DSP

Linked Data

• COSMIC: COSM3162644
• MyVariant Identifiers: chr6:g.7574950T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7574717T>G , CM000668.2:g.7574717T>G	GRCh38
NC_000006.11:g.7574950T>G , CM000668.1:g.7574950T>G	GRCh37
NC_000006.10:g.7519949T>G	NCBI36
NG_008803.1:g.38081T>G , LRG_423:g.38081T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.2358T>G	ENSP00000518230.1:p.Val786=
ENST00000684395.1:n.999T>G
ENST00000379802.8:c.2358T>G MANE Select	ENSP00000369129.3:p.Val786=
ENST00000379802.7:c.2358T>G	ENSP00000369129.3:p.Val786=
ENST00000418664.2:c.2358T>G	ENSP00000396591.2:p.Val786=
NM_001008844.1:c.2358T>G	NP_001008844.1:p.Val786=
NM_004415.2:c.2358T>G , LRG_423t1:c.2358T>G	NP_004406.2:p.Val786=
XM_011514323.1:c.2358T>G	XP_011512625.1:p.Val786=
NM_001008844.2:c.2358T>G	NP_001008844.1:p.Val786=
NM_001319034.1:c.2358T>G	NP_001305963.1:p.Val786=
NM_004415.3:c.2358T>G	NP_004406.2:p.Val786=
NM_004415.4:c.2358T>G MANE Select	NP_004406.2:p.Val786=
NM_001008844.3:c.2358T>G	NP_001008844.1:p.Val786=
NM_001319034.2:c.2358T>G	NP_001305963.1:p.Val786=