Canonical Allele Identifier: CA448517708

Gene: DSP

Linked Data

• MyVariant Identifiers: chr6:g.7565597G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565364G>C , CM000668.2:g.7565364G>C	GRCh38
NC_000006.11:g.7565597G>C , CM000668.1:g.7565597G>C	GRCh37
NC_000006.10:g.7510596G>C	NCBI36
NG_008803.1:g.28728G>C , LRG_423:g.28728G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.783G>C	ENSP00000518230.1:p.Ala261=
ENST00000682228.1:n.107G>C
ENST00000379802.8:c.783G>C MANE Select	ENSP00000369129.3:p.Ala261=
ENST00000379802.7:c.783G>C	ENSP00000369129.3:p.Ala261=
ENST00000418664.2:c.783G>C	ENSP00000396591.2:p.Ala261=
ENST00000506617.1:n.301G>C
NM_001008844.1:c.783G>C	NP_001008844.1:p.Ala261=
NM_004415.2:c.783G>C , LRG_423t1:c.783G>C	NP_004406.2:p.Ala261=
XM_011514323.1:c.783G>C	XP_011512625.1:p.Ala261=
NM_001008844.2:c.783G>C	NP_001008844.1:p.Ala261=
NM_001319034.1:c.783G>C	NP_001305963.1:p.Ala261=
NM_004415.3:c.783G>C	NP_004406.2:p.Ala261=
NM_004415.4:c.783G>C MANE Select	NP_004406.2:p.Ala261=
NM_001008844.3:c.783G>C	NP_001008844.1:p.Ala261=
NM_001319034.2:c.783G>C	NP_001305963.1:p.Ala261=