Canonical Allele Identifier: CA2677220284

Gene: DSP

Linked Data

• gnomAD v4: 6-7565750-T-TCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565750_7565751insCA , CM000668.2:g.7565750_7565751insCA	GRCh38
NC_000006.11:g.7565983_7565984insCA , CM000668.1:g.7565983_7565984insCA	GRCh37
NC_000006.10:g.7510982_7510983insCA	NCBI36
NG_008803.1:g.29114_29115insCA , LRG_423:g.29114_29115insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.939+230_939+231insCA	ENSP00000518230.1:n.939+230_939+231insCA
ENST00000682228.1:n.263+230_263+231insCA
ENST00000379802.8:c.939+230_939+231insCA MANE Select	ENSP00000369129.3:n.939+230_939+231insCA
ENST00000379802.7:c.939+230_939+231insCA	ENSP00000369129.3:n.939+230_939+231insCA
ENST00000418664.2:c.939+230_939+231insCA	ENSP00000396591.2:n.939+230_939+231insCA
ENST00000506617.1:n.687_688insCA
NM_001008844.1:c.939+230_939+231insCA	NP_001008844.1:n.939+230_939+231insCA
NM_004415.2:c.939+230_939+231insCA , LRG_423t1:c.939+230_939+231insCA	NP_004406.2:n.939+230_939+231insCA
XM_011514323.1:c.939+230_939+231insCA	XP_011512625.1:n.939+230_939+231insCA
NM_001008844.2:c.939+230_939+231insCA	NP_001008844.1:n.939+230_939+231insCA
NM_001319034.1:c.939+230_939+231insCA	NP_001305963.1:n.939+230_939+231insCA
NM_004415.3:c.939+230_939+231insCA	NP_004406.2:n.939+230_939+231insCA
NM_004415.4:c.939+230_939+231insCA MANE Select	NP_004406.2:n.939+230_939+231insCA
NM_001008844.3:c.939+230_939+231insCA	NP_001008844.1:n.939+230_939+231insCA
NM_001319034.2:c.939+230_939+231insCA	NP_001305963.1:n.939+230_939+231insCA