Canonical Allele Identifier: CA448716842

Gene: DSP

Linked Data

• dbSNP Id: rs756052276
• gnomAD v2: 6-7585370-A-C
• gnomAD v4: 6-7585137-A-C
• MyVariant Identifiers: chr6:g.7585370A>C (hg19) ; chr6:g.7585137A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585137A>C , CM000668.2:g.7585137A>C	GRCh38
NC_000006.11:g.7585370A>C , CM000668.1:g.7585370A>C	GRCh37
NC_000006.10:g.7530369A>C	NCBI36
NG_008803.1:g.48501A>C , LRG_423:g.48501A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6546A>C	ENSP00000518230.1:p.Thr2182=
ENST00000379802.8:c.7875A>C MANE Select	ENSP00000369129.3:p.Thr2625=
ENST00000379802.7:c.7875A>C	ENSP00000369129.3:p.Thr2625=
ENST00000418664.2:c.6078A>C	ENSP00000396591.2:p.Thr2026=
NM_001008844.1:c.6078A>C	NP_001008844.1:p.Thr2026=
NM_004415.2:c.7875A>C , LRG_423t1:c.7875A>C	NP_004406.2:p.Thr2625=
XM_011514323.1:c.6546A>C	XP_011512625.1:p.Thr2182=
NM_001008844.2:c.6078A>C	NP_001008844.1:p.Thr2026=
NM_001319034.1:c.6546A>C	NP_001305963.1:p.Thr2182=
NM_004415.3:c.7875A>C	NP_004406.2:p.Thr2625=
NM_004415.4:c.7875A>C MANE Select	NP_004406.2:p.Thr2625=
NM_001008844.3:c.6078A>C	NP_001008844.1:p.Thr2026=
NM_001319034.2:c.6546A>C	NP_001305963.1:p.Thr2182=