Canonical Allele Identifier: CA2576480507
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524593_31524594insACC , CM000680.2:g.31524593_31524594insACC GRCh38
NC_000018.9:g.29104556_29104557insACC , CM000680.1:g.29104556_29104557insACC GRCh37
NC_000018.8:g.27358554_27358555insACC NCBI36
NG_007072.3:g.31352_31353insACC , LRG_397:g.31352_31353insACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000682087.2:n.659+8_659+9insACC
ENST00000683614.2:n.659+8_659+9insACC
ENST00000682087.1:c.659+8_659+9insACC
ENST00000683614.1:c.659+8_659+9insACC
ENST00000261590.13:c.828+8_828+9insACC MANE Select ENSP00000261590.8:n.828+8_828+9insACC
ENST00000261590.12:c.828+8_828+9insACC ENSP00000261590.8:n.828+8_828+9insACC
NM_001943.3:c.828+8_828+9insACC , LRG_397t1:c.828+8_828+9insACC NP_001934.2:n.828+8_828+9insACC
NM_001943.4:c.828+8_828+9insACC NP_001934.2:n.828+8_828+9insACC
XM_024451095.1:c.294+8_294+9insACC XP_024306863.1:n.294+8_294+9insACC
NM_001943.5:c.828+8_828+9insACC MANE Select NP_001934.2:n.828+8_828+9insACC