Canonical Allele Identifier: CA2677220018

Gene: DSP

Linked Data

• gnomAD v4: 6-7565649-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565649G>T , CM000668.2:g.7565649G>T	GRCh38
NC_000006.11:g.7565882G>T , CM000668.1:g.7565882G>T	GRCh37
NC_000006.10:g.7510881G>T	NCBI36
NG_008803.1:g.29013G>T , LRG_423:g.29013G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.939+129G>T	ENSP00000518230.1:n.939+129G>T
ENST00000682228.1:n.263+129G>T
ENST00000379802.8:c.939+129G>T MANE Select	ENSP00000369129.3:n.939+129G>T
ENST00000379802.7:c.939+129G>T	ENSP00000369129.3:n.939+129G>T
ENST00000418664.2:c.939+129G>T	ENSP00000396591.2:n.939+129G>T
ENST00000506617.1:n.586G>T
NM_001008844.1:c.939+129G>T	NP_001008844.1:n.939+129G>T
NM_004415.2:c.939+129G>T , LRG_423t1:c.939+129G>T	NP_004406.2:n.939+129G>T
XM_011514323.1:c.939+129G>T	XP_011512625.1:n.939+129G>T
NM_001008844.2:c.939+129G>T	NP_001008844.1:n.939+129G>T
NM_001319034.1:c.939+129G>T	NP_001305963.1:n.939+129G>T
NM_004415.3:c.939+129G>T	NP_004406.2:n.939+129G>T
NM_004415.4:c.939+129G>T MANE Select	NP_004406.2:n.939+129G>T
NM_001008844.3:c.939+129G>T	NP_001008844.1:n.939+129G>T
NM_001319034.2:c.939+129G>T	NP_001305963.1:n.939+129G>T