Canonical Allele Identifier: CA448717205

Gene: DSP

Linked Data

• dbSNP Id: rs1199053877
• gnomAD v2: 6-7585943-T-C
• gnomAD v4: 6-7585710-T-C
• MyVariant Identifiers: chr6:g.7585943T>C (hg19) ; chr6:g.7585710T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585710T>C , CM000668.2:g.7585710T>C	GRCh38
NC_000006.11:g.7585943T>C , CM000668.1:g.7585943T>C	GRCh37
NC_000006.10:g.7530942T>C	NCBI36
NG_008803.1:g.49074T>C , LRG_423:g.49074T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.7119T>C	ENSP00000518230.1:p.Pro2373=
ENST00000379802.8:c.8448T>C MANE Select	ENSP00000369129.3:p.Pro2816=
ENST00000379802.7:c.8448T>C	ENSP00000369129.3:p.Pro2816=
ENST00000418664.2:c.6651T>C	ENSP00000396591.2:p.Pro2217=
NM_001008844.1:c.6651T>C	NP_001008844.1:p.Pro2217=
NM_004415.2:c.8448T>C , LRG_423t1:c.8448T>C	NP_004406.2:p.Pro2816=
XM_011514323.1:c.7119T>C	XP_011512625.1:p.Pro2373=
NM_001008844.2:c.6651T>C	NP_001008844.1:p.Pro2217=
NM_001319034.1:c.7119T>C	NP_001305963.1:p.Pro2373=
NM_004415.3:c.8448T>C	NP_004406.2:p.Pro2816=
NM_004415.4:c.8448T>C MANE Select	NP_004406.2:p.Pro2816=
NM_001008844.3:c.6651T>C	NP_001008844.1:p.Pro2217=
NM_001319034.2:c.7119T>C	NP_001305963.1:p.Pro2373=