Canonical Allele Identifier: CA2000618362

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112230222C= , CM000673.2:g.112230222C=	GRCh38
NC_000011.9:g.112100945C= , CM000673.1:g.112100945C=	GRCh37
NC_000011.8:g.111606155C=	NCBI36
NG_008743.1:g.8858C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.178C= MANE Select	ENSP00000280362.3:p.His60=
ENST00000280362.7:c.178C=	ENSP00000280362.3:p.His60=
ENST00000524931.1:c.-27C=	ENSP00000434688.1:n.-27C=
ENST00000525803.1:c.163+1549C=	ENSP00000431750.1:n.163+1549C=
ENST00000528679.5:c.164-404C=	ENSP00000435895.1:n.164-404C=
ENST00000531175.1:n.129C=
ENST00000531673.5:c.164-404C=	ENSP00000433469.1:n.164-404C=
NM_000317.2:c.178C=	NP_000308.1:p.His60=
XM_011542943.1:c.139C=	XP_011541245.1:p.His47=
NM_000317.3:c.178C= MANE Select	NP_000308.1:p.His60=