Canonical Allele Identifier: CA402139676
Gene: DSG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31541272G>C , CM000680.2:g.31541272G>C GRCh38
NC_000018.9:g.29121235G>C , CM000680.1:g.29121235G>C GRCh37
NC_000018.8:g.27375233G>C NCBI36
NG_007072.3:g.48031G>C , LRG_397:g.48031G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.1959G>C MANE Select ENSP00000261590.8:p.Met653Ile
ENST00000261590.12:c.1959G>C ENSP00000261590.8:p.Met653Ile
NM_001943.3:c.1959G>C , LRG_397t1:c.1959G>C NP_001934.2:p.Met653Ile
NM_001943.4:c.1959G>C NP_001934.2:p.Met653Ile
XM_024451095.1:c.1425G>C XP_024306863.1:p.Met475Ile
NM_001943.5:c.1959G>C MANE Select NP_001934.2:p.Met653Ile