Canonical Allele Identifier: CA2293855886

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31522179_31522185delinsATCCTCC , CM000680.2:g.31522179_31522185delinsATCCTCC	GRCh38
NC_000018.9:g.29102142_29102148delinsATCCTCC , CM000680.1:g.29102142_29102148delinsATCCTCC	GRCh37
NC_000018.8:g.27356140_27356146delinsATCCTCC	NCBI36
NG_007072.3:g.28938_28944delinsATCCTCC , LRG_397:g.28938_28944delinsATCCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682087.2:n.451_457delinsATCCTCC
ENST00000682241.2:c.620_626delinsATCCTCC	ENSP00000507600.2:p.Tyr207=
ENST00000683614.2:n.451_457delinsATCCTCC
ENST00000682087.1:c.451_457delinsATCCTCC
ENST00000682241.1:c.451_457delinsATCCTCC
ENST00000683614.1:c.451_457delinsATCCTCC
ENST00000683654.1:c.620_626delinsATCCTCC	ENSP00000506971.1:p.Tyr207=
ENST00000684461.1:n.1290_1296delinsATCCTCC
ENST00000261590.13:c.620_626delinsATCCTCC MANE Select	ENSP00000261590.8:p.Tyr207=
ENST00000261590.12:c.620_626delinsATCCTCC	ENSP00000261590.8:p.Tyr207=
ENST00000585206.1:c.620_626delinsATCCTCC	ENSP00000462503.1:p.Tyr207=
NM_001943.3:c.620_626delinsATCCTCC , LRG_397t1:c.620_626delinsATCCTCC	NP_001934.2:p.Tyr207=
NM_001943.4:c.620_626delinsATCCTCC	NP_001934.2:p.Tyr207=
XM_024451095.1:c.86_92delinsATCCTCC	XP_024306863.1:p.Tyr29=
NM_001943.5:c.620_626delinsATCCTCC MANE Select	NP_001934.2:p.Tyr207=