Canonical Allele Identifier: CA2000619942
Gene: PTS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112233477_112233491delinsAGTTCTTCCTGTAGG , CM000673.2:g.112233477_112233491delinsAGTTCTTCCTGTAGG GRCh38
NC_000011.9:g.112104200_112104214delinsAGTTCTTCCTGTAGG , CM000673.1:g.112104200_112104214delinsAGTTCTTCCTGTAGG GRCh37
NC_000011.8:g.111609410_111609424delinsAGTTCTTCCTGTAGG NCBI36
NG_008743.1:g.12113_12127delinsAGTTCTTCCTGTAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000280362.8:c.360_374delinsAGTTCTTCCTGTAGG MANE Select ENSP00000280362.3:p.Lys120=
ENST00000280362.7:c.360_374delinsAGTTCTTCCTGTAGG ENSP00000280362.3:p.Lys120=
ENST00000524931.1:c.156_170delinsAGTTCTTCCTGTAGG ENSP00000434688.1:p.Lys52=
ENST00000525803.1:c.*94_*108delinsAGTTCTTCCTGTAGG ENSP00000431750.1:n.*94_*108delinsAGTTCTT...
ENST00000527428.5:n.488+244_488+258delinsAGTTCTTCCTGTAGG
ENST00000527635.1:n.401_415delinsAGTTCTTCCTGTAGG
ENST00000528679.5:c.*169_*183delinsAGTTCTTCCTGTAGG ENSP00000435895.1:n.*169_*183delinsAGTTCT...
ENST00000531673.5:c.*123+244_*123+258delinsAGTTCTTCCTGTAGG ENSP00000433469.1:n.*123+244_*123+258deli...
NM_000317.2:c.360_374delinsAGTTCTTCCTGTAGG NP_000308.1:p.Lys120=
XM_011542943.1:c.321_335delinsAGTTCTTCCTGTAGG XP_011541245.1:p.Lys107=
NM_000317.3:c.360_374delinsAGTTCTTCCTGTAGG MANE Select NP_000308.1:p.Lys120=