Canonical Allele Identifier: CA2769905066

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565276del , CM000668.2:g.7565276del	GRCh38
NC_000006.11:g.7565509del , CM000668.1:g.7565509del	GRCh37
NC_000006.10:g.7510508del	NCBI36
NG_008803.1:g.28640del , LRG_423:g.28640del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.778-83del	ENSP00000518230.1:n.778-83del
ENST00000682228.1:n.19del
ENST00000379802.8:c.778-83del MANE Select	ENSP00000369129.3:n.778-83del
ENST00000379802.7:c.778-83del	ENSP00000369129.3:n.778-83del
ENST00000418664.2:c.778-83del	ENSP00000396591.2:n.778-83del
ENST00000506617.1:n.296-83del
NM_001008844.1:c.778-83del	NP_001008844.1:n.778-83del
NM_004415.2:c.778-83del , LRG_423t1:c.778-83del	NP_004406.2:n.778-83del
XM_011514323.1:c.778-83del	XP_011512625.1:n.778-83del
NM_001008844.2:c.778-83del	NP_001008844.1:n.778-83del
NM_001319034.1:c.778-83del	NP_001305963.1:n.778-83del
NM_004415.3:c.778-83del	NP_004406.2:n.778-83del
NM_004415.4:c.778-83del MANE Select	NP_004406.2:n.778-83del
NM_001008844.3:c.778-83del	NP_001008844.1:n.778-83del
NM_001319034.2:c.778-83del	NP_001305963.1:n.778-83del