Canonical Allele Identifier: CA2677219495

Gene: DSP

Linked Data

• gnomAD v4: 6-7565270-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565270A>G , CM000668.2:g.7565270A>G	GRCh38
NC_000006.11:g.7565503A>G , CM000668.1:g.7565503A>G	GRCh37
NC_000006.10:g.7510502A>G	NCBI36
NG_008803.1:g.28634A>G , LRG_423:g.28634A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.778-89A>G	ENSP00000518230.1:n.778-89A>G
ENST00000682228.1:n.13A>G
ENST00000379802.8:c.778-89A>G MANE Select	ENSP00000369129.3:n.778-89A>G
ENST00000379802.7:c.778-89A>G	ENSP00000369129.3:n.778-89A>G
ENST00000418664.2:c.778-89A>G	ENSP00000396591.2:n.778-89A>G
ENST00000506617.1:n.296-89A>G
NM_001008844.1:c.778-89A>G	NP_001008844.1:n.778-89A>G
NM_004415.2:c.778-89A>G , LRG_423t1:c.778-89A>G	NP_004406.2:n.778-89A>G
XM_011514323.1:c.778-89A>G	XP_011512625.1:n.778-89A>G
NM_001008844.2:c.778-89A>G	NP_001008844.1:n.778-89A>G
NM_001319034.1:c.778-89A>G	NP_001305963.1:n.778-89A>G
NM_004415.3:c.778-89A>G	NP_004406.2:n.778-89A>G
NM_004415.4:c.778-89A>G MANE Select	NP_004406.2:n.778-89A>G
NM_001008844.3:c.778-89A>G	NP_001008844.1:n.778-89A>G
NM_001319034.2:c.778-89A>G	NP_001305963.1:n.778-89A>G