Canonical Allele Identifier: CA778421834
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1258412075

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31542507_31542510dup , CM000680.2:g.31542507_31542510dup GRCh38
NC_000018.9:g.29122470_29122473dup , CM000680.1:g.29122470_29122473dup GRCh37
NC_000018.8:g.27376468_27376471dup NCBI36
NG_007072.3:g.49266_49269dup , LRG_397:g.49266_49269dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2002-13_2002-10dup (DSG2) MANE Select ENSP00000261590.8:n.2002-13_2002-10dup
ENST00000261590.12:c.2002-13_2002-10dup (DSG2) ENSP00000261590.8:n.2002-13_2002-10dup
NM_001943.3:c.2002-13_2002-10dup , LRG_397t1:c.2002-13_2002-10dup (DSG2) NP_001934.2:n.2002-13_2002-10dup
NR_045216.1:n.1811-187_1811-184dup (DSG2-AS1)
NM_001943.4:c.2002-13_2002-10dup (DSG2) NP_001934.2:n.2002-13_2002-10dup
XM_024451095.1:c.1468-13_1468-10dup (DSG2) XP_024306863.1:n.1468-13_1468-10dup
NM_001943.5:c.2002-13_2002-10dup (DSG2) MANE Select NP_001934.2:n.2002-13_2002-10dup