Canonical Allele Identifier: CA448716542

Gene: DSP

Linked Data

• MyVariant Identifiers: chr6:g.7585292C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585059C>A , CM000668.2:g.7585059C>A	GRCh38
NC_000006.11:g.7585292C>A , CM000668.1:g.7585292C>A	GRCh37
NC_000006.10:g.7530291C>A	NCBI36
NG_008803.1:g.48423C>A , LRG_423:g.48423C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6468C>A	ENSP00000518230.1:p.Val2156=
ENST00000379802.8:c.7797C>A MANE Select	ENSP00000369129.3:p.Val2599=
ENST00000379802.7:c.7797C>A	ENSP00000369129.3:p.Val2599=
ENST00000418664.2:c.6000C>A	ENSP00000396591.2:p.Val2000=
NM_001008844.1:c.6000C>A	NP_001008844.1:p.Val2000=
NM_004415.2:c.7797C>A , LRG_423t1:c.7797C>A	NP_004406.2:p.Val2599=
XM_011514323.1:c.6468C>A	XP_011512625.1:p.Val2156=
NM_001008844.2:c.6000C>A	NP_001008844.1:p.Val2000=
NM_001319034.1:c.6468C>A	NP_001305963.1:p.Val2156=
NM_004415.3:c.7797C>A	NP_004406.2:p.Val2599=
NM_004415.4:c.7797C>A MANE Select	NP_004406.2:p.Val2599=
NM_001008844.3:c.6000C>A	NP_001008844.1:p.Val2000=
NM_001319034.2:c.6468C>A	NP_001305963.1:p.Val2156=