Canonical Allele Identifier: CA448531285

Gene: DSP

Linked Data

• dbSNP Id: rs1759652125
• MyVariant Identifiers: chr6:g.7586033G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585800G>C , CM000668.2:g.7585800G>C	GRCh38
NC_000006.11:g.7586033G>C , CM000668.1:g.7586033G>C	GRCh37
NC_000006.10:g.7531032G>C	NCBI36
NG_008803.1:g.49164G>C , LRG_423:g.49164G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.7209G>C	ENSP00000518230.1:p.Arg2403=
ENST00000379802.8:c.8538G>C MANE Select	ENSP00000369129.3:p.Arg2846=
ENST00000379802.7:c.8538G>C	ENSP00000369129.3:p.Arg2846=
ENST00000418664.2:c.6741G>C	ENSP00000396591.2:p.Arg2247=
NM_001008844.1:c.6741G>C	NP_001008844.1:p.Arg2247=
NM_004415.2:c.8538G>C , LRG_423t1:c.8538G>C	NP_004406.2:p.Arg2846=
XM_011514323.1:c.7209G>C	XP_011512625.1:p.Arg2403=
NM_001008844.2:c.6741G>C	NP_001008844.1:p.Arg2247=
NM_001319034.1:c.7209G>C	NP_001305963.1:p.Arg2403=
NM_004415.3:c.8538G>C	NP_004406.2:p.Arg2846=
NM_004415.4:c.8538G>C MANE Select	NP_004406.2:p.Arg2846=
NM_001008844.3:c.6741G>C	NP_001008844.1:p.Arg2247=
NM_001319034.2:c.7209G>C	NP_001305963.1:p.Arg2403=