Canonical Allele Identifier: CA402135356
Gene: DSG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524702G>C , CM000680.2:g.31524702G>C GRCh38
NC_000018.9:g.29104665G>C , CM000680.1:g.29104665G>C GRCh37
NC_000018.8:g.27358663G>C NCBI36
NG_007072.3:g.31461G>C , LRG_397:g.31461G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682087.2:n.660-1G>C
ENST00000683614.2:n.660-1G>C
ENST00000682087.1:c.660-1G>C
ENST00000683614.1:c.660-1G>C
ENST00000261590.13:c.829-1G>C MANE Select ENSP00000261590.8:n.829-1G>C
ENST00000261590.12:c.829-1G>C ENSP00000261590.8:n.829-1G>C
NM_001943.3:c.829-1G>C , LRG_397t1:c.829-1G>C NP_001934.2:n.829-1G>C
NM_001943.4:c.829-1G>C NP_001934.2:n.829-1G>C
XM_024451095.1:c.295-1G>C XP_024306863.1:n.295-1G>C
NM_001943.5:c.829-1G>C MANE Select NP_001934.2:n.829-1G>C