Canonical Allele Identifier: CA2293866303
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546692_31546696delinsATCTT , CM000680.2:g.31546692_31546696delinsATCTT GRCh38
NC_000018.9:g.29126655_29126659delinsATCTT , CM000680.1:g.29126655_29126659delinsATCTT GRCh37
NC_000018.8:g.27380653_27380657delinsATCTT NCBI36
NG_007072.3:g.53451_53455delinsATCTT , LRG_397:g.53451_53455delinsATCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3306_3310delinsATCTT (DSG2) MANE Select ENSP00000261590.8:p.Thr1102=
ENST00000261590.12:c.3306_3310delinsATCTT (DSG2) ENSP00000261590.8:p.Thr1102=
NM_001943.3:c.3306_3310delinsATCTT , LRG_397t1:c.3306_3310delinsATCTT (DSG2) NP_001934.2:p.Thr1102=
NR_045216.1:n.1346-790_1346-786delinsAAGAT (DSG2-AS1)
NM_001943.4:c.3306_3310delinsATCTT (DSG2) NP_001934.2:p.Thr1102=
XM_024451095.1:c.2772_2776delinsATCTT (DSG2) XP_024306863.1:p.Thr924=
NM_001943.5:c.3306_3310delinsATCTT (DSG2) MANE Select NP_001934.2:p.Thr1102=