Canonical Allele Identifier: CA2812003871
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31542876dup , CM000680.2:g.31542876dup GRCh38
NC_000018.9:g.29122839dup , CM000680.1:g.29122839dup GRCh37
NC_000018.8:g.27376837dup NCBI36
NG_007072.3:g.49635dup , LRG_397:g.49635dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2334+24dup (DSG2) MANE Select ENSP00000261590.8:n.2334+24dup
ENST00000261590.12:c.2334+24dup (DSG2) ENSP00000261590.8:n.2334+24dup
NM_001943.3:c.2334+24dup , LRG_397t1:c.2334+24dup (DSG2) NP_001934.2:n.2334+24dup
NR_045216.1:n.1810+227dup (DSG2-AS1)
NM_001943.4:c.2334+24dup (DSG2) NP_001934.2:n.2334+24dup
XM_024451095.1:c.1800+24dup (DSG2) XP_024306863.1:n.1800+24dup
NM_001943.5:c.2334+24dup (DSG2) MANE Select NP_001934.2:n.2334+24dup