Canonical Allele Identifier: CA053129

Gene: DSP

Linked Data

• dbSNP Id: rs749028057
• ExAC: 6:7565778 G / A
• gnomAD v2: 6-7565778-G-A
• gnomAD v3: 6-7565545-G-A
• gnomAD v4: 6-7565545-G-A
• MyVariant Identifiers: chr6:g.7565778G>A (hg19) ; chr6:g.7565545G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565545G>A , CM000668.2:g.7565545G>A	GRCh38
NC_000006.11:g.7565778G>A , CM000668.1:g.7565778G>A	GRCh37
NC_000006.10:g.7510777G>A	NCBI36
NG_008803.1:g.28909G>A , LRG_423:g.28909G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.939+25G>A	ENSP00000518230.1:n.939+25G>A
ENST00000682228.1:n.263+25G>A
ENST00000379802.8:c.939+25G>A MANE Select	ENSP00000369129.3:n.939+25G>A
ENST00000379802.7:c.939+25G>A	ENSP00000369129.3:n.939+25G>A
ENST00000418664.2:c.939+25G>A	ENSP00000396591.2:n.939+25G>A
ENST00000506617.1:n.482G>A
NM_001008844.1:c.939+25G>A	NP_001008844.1:n.939+25G>A
NM_004415.2:c.939+25G>A , LRG_423t1:c.939+25G>A	NP_004406.2:n.939+25G>A
XM_011514323.1:c.939+25G>A	XP_011512625.1:n.939+25G>A
NM_001008844.2:c.939+25G>A	NP_001008844.1:n.939+25G>A
NM_001319034.1:c.939+25G>A	NP_001305963.1:n.939+25G>A
NM_004415.3:c.939+25G>A	NP_004406.2:n.939+25G>A
NM_004415.4:c.939+25G>A MANE Select	NP_004406.2:n.939+25G>A
NM_001008844.3:c.939+25G>A	NP_001008844.1:n.939+25G>A
NM_001319034.2:c.939+25G>A	NP_001305963.1:n.939+25G>A