Canonical Allele Identifier: CA2677220041

Gene: DSP

Linked Data

• gnomAD v4: 6-7565659-ATCCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565668_7565671del , CM000668.2:g.7565668_7565671del	GRCh38
NC_000006.11:g.7565901_7565904del , CM000668.1:g.7565901_7565904del	GRCh37
NC_000006.10:g.7510900_7510903del	NCBI36
NG_008803.1:g.29032_29035del , LRG_423:g.29032_29035del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.939+148_939+151del	ENSP00000518230.1:n.939+148_939+151del
ENST00000682228.1:n.263+148_263+151del
ENST00000379802.8:c.939+148_939+151del MANE Select	ENSP00000369129.3:n.939+148_939+151del
ENST00000379802.7:c.939+148_939+151del	ENSP00000369129.3:n.939+148_939+151del
ENST00000418664.2:c.939+148_939+151del	ENSP00000396591.2:n.939+148_939+151del
ENST00000506617.1:n.605_608del
NM_001008844.1:c.939+148_939+151del	NP_001008844.1:n.939+148_939+151del
NM_004415.2:c.939+148_939+151del , LRG_423t1:c.939+148_939+151del	NP_004406.2:n.939+148_939+151del
XM_011514323.1:c.939+148_939+151del	XP_011512625.1:n.939+148_939+151del
NM_001008844.2:c.939+148_939+151del	NP_001008844.1:n.939+148_939+151del
NM_001319034.1:c.939+148_939+151del	NP_001305963.1:n.939+148_939+151del
NM_004415.3:c.939+148_939+151del	NP_004406.2:n.939+148_939+151del
NM_004415.4:c.939+148_939+151del MANE Select	NP_004406.2:n.939+148_939+151del
NM_001008844.3:c.939+148_939+151del	NP_001008844.1:n.939+148_939+151del
NM_001319034.2:c.939+148_939+151del	NP_001305963.1:n.939+148_939+151del