Canonical Allele Identifier: CA2576480591
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31542877_31542883del , CM000680.2:g.31542877_31542883del GRCh38
NC_000018.9:g.29122840_29122846del , CM000680.1:g.29122840_29122846del GRCh37
NC_000018.8:g.27376838_27376844del NCBI36
NG_007072.3:g.49636_49642del , LRG_397:g.49636_49642del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2334+25_2334+31del (DSG2) MANE Select ENSP00000261590.8:n.2334+25_2334+31del
ENST00000261590.12:c.2334+25_2334+31del (DSG2) ENSP00000261590.8:n.2334+25_2334+31del
NM_001943.3:c.2334+25_2334+31del , LRG_397t1:c.2334+25_2334+31del (DSG2) NP_001934.2:n.2334+25_2334+31del
NR_045216.1:n.1810+221_1810+227del (DSG2-AS1)
NM_001943.4:c.2334+25_2334+31del (DSG2) NP_001934.2:n.2334+25_2334+31del
XM_024451095.1:c.1800+25_1800+31del (DSG2) XP_024306863.1:n.1800+25_1800+31del
NM_001943.5:c.2334+25_2334+31del (DSG2) MANE Select NP_001934.2:n.2334+25_2334+31del