Canonical Allele Identifier: CA2641407657
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546522_31546525del , CM000680.2:g.31546522_31546525del GRCh38
NC_000018.9:g.29126485_29126488del , CM000680.1:g.29126485_29126488del GRCh37
NC_000018.8:g.27380483_27380486del NCBI36
NG_007072.3:g.53281_53284del , LRG_397:g.53281_53284del

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.3136_3139del (DSG2) MANE Select ENSP00000261590.8:p.Val1046GlnfsTer5
ENST00000261590.12:c.3136_3139del (DSG2) ENSP00000261590.8:p.Val1046GlnfsTer5
NM_001943.3:c.3136_3139del , LRG_397t1:c.3136_3139del (DSG2) NP_001934.2:p.Val1046GlnfsTer5
NR_045216.1:n.1346-618_1346-615del (DSG2-AS1)
NM_001943.4:c.3136_3139del (DSG2) NP_001934.2:p.Val1046GlnfsTer5
XM_024451095.1:c.2602_2605del (DSG2) XP_024306863.1:p.Val868GlnfsTer5
NM_001943.5:c.3136_3139del (DSG2) MANE Select NP_001934.2:p.Val1046GlnfsTer5