Canonical Allele Identifier: CA133954898

Gene: DSP

Linked Data

• dbSNP Id: rs555012096
• gnomAD v2: 6-7565943-CT-C
• gnomAD v3: 6-7565710-CT-C
• gnomAD v4: 6-7565710-CT-C
• MyVariant Identifiers: chr6:g.7565944del (hg19) ; chr6:g.7565711del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565712del , CM000668.2:g.7565712del	GRCh38
NC_000006.11:g.7565945del , CM000668.1:g.7565945del	GRCh37
NC_000006.10:g.7510944del	NCBI36
NG_008803.1:g.29076del , LRG_423:g.29076del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.939+192del	ENSP00000518230.1:n.939+192del
ENST00000682228.1:n.263+192del
ENST00000379802.8:c.939+192del MANE Select	ENSP00000369129.3:n.939+192del
ENST00000379802.7:c.939+192del	ENSP00000369129.3:n.939+192del
ENST00000418664.2:c.939+192del	ENSP00000396591.2:n.939+192del
ENST00000506617.1:n.649del
NM_001008844.1:c.939+192del	NP_001008844.1:n.939+192del
NM_004415.2:c.939+192del , LRG_423t1:c.939+192del	NP_004406.2:n.939+192del
XM_011514323.1:c.939+192del	XP_011512625.1:n.939+192del
NM_001008844.2:c.939+192del	NP_001008844.1:n.939+192del
NM_001319034.1:c.939+192del	NP_001305963.1:n.939+192del
NM_004415.3:c.939+192del	NP_004406.2:n.939+192del
NM_004415.4:c.939+192del MANE Select	NP_004406.2:n.939+192del
NM_001008844.3:c.939+192del	NP_001008844.1:n.939+192del
NM_001319034.2:c.939+192del	NP_001305963.1:n.939+192del