Canonical Allele Identifier: CA2677220029

Gene: DSP

Linked Data

• gnomAD v4: 6-7565654-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565659dup , CM000668.2:g.7565659dup	GRCh38
NC_000006.11:g.7565892dup , CM000668.1:g.7565892dup	GRCh37
NC_000006.10:g.7510891dup	NCBI36
NG_008803.1:g.29023dup , LRG_423:g.29023dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.939+139dup	ENSP00000518230.1:n.939+139dup
ENST00000682228.1:n.263+139dup
ENST00000379802.8:c.939+139dup MANE Select	ENSP00000369129.3:n.939+139dup
ENST00000379802.7:c.939+139dup	ENSP00000369129.3:n.939+139dup
ENST00000418664.2:c.939+139dup	ENSP00000396591.2:n.939+139dup
ENST00000506617.1:n.596dup
NM_001008844.1:c.939+139dup	NP_001008844.1:n.939+139dup
NM_004415.2:c.939+139dup , LRG_423t1:c.939+139dup	NP_004406.2:n.939+139dup
XM_011514323.1:c.939+139dup	XP_011512625.1:n.939+139dup
NM_001008844.2:c.939+139dup	NP_001008844.1:n.939+139dup
NM_001319034.1:c.939+139dup	NP_001305963.1:n.939+139dup
NM_004415.3:c.939+139dup	NP_004406.2:n.939+139dup
NM_004415.4:c.939+139dup MANE Select	NP_004406.2:n.939+139dup
NM_001008844.3:c.939+139dup	NP_001008844.1:n.939+139dup
NM_001319034.2:c.939+139dup	NP_001305963.1:n.939+139dup