Canonical Allele Identifier: CA2000617577

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112228537_112228538delinsAG , CM000673.2:g.112228537_112228538delinsAG	GRCh38
NC_000011.9:g.112099260_112099261delinsAG , CM000673.1:g.112099260_112099261delinsAG	GRCh37
NC_000011.8:g.111604470_111604471delinsAG	NCBI36
NG_008743.1:g.7173_7174delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.84-57_84-56delinsAG MANE Select	ENSP00000280362.3:n.84-57_84-56delinsAG
ENST00000280362.7:c.84-57_84-56delinsAG	ENSP00000280362.3:n.84-57_84-56delinsAG
ENST00000524931.1:c.-121-57_-121-56delinsAG	ENSP00000434688.1:n.-121-57_-121-56delinsAG
ENST00000525645.1:n.159-57_159-56delinsAG
ENST00000525803.1:c.84-57_84-56delinsAG	ENSP00000431750.1:n.84-57_84-56delinsAG
ENST00000528679.5:c.84-57_84-56delinsAG	ENSP00000435895.1:n.84-57_84-56delinsAG
ENST00000531673.5:c.84-57_84-56delinsAG	ENSP00000433469.1:n.84-57_84-56delinsAG
NM_000317.2:c.84-57_84-56delinsAG	NP_000308.1:n.84-57_84-56delinsAG
NM_000317.3:c.84-57_84-56delinsAG MANE Select	NP_000308.1:n.84-57_84-56delinsAG