Canonical Allele Identifier: CA2000616551

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112226504A= , CM000673.2:g.112226504A=	GRCh38
NC_000011.9:g.112097227A= , CM000673.1:g.112097227A=	GRCh37
NC_000011.8:g.111602437A=	NCBI36
NG_008743.1:g.5140A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000280362.8:c.61A= MANE Select	ENSP00000280362.3:p.Ser21=
ENST00000280362.7:c.61A=	ENSP00000280362.3:p.Ser21=
ENST00000525645.1:n.136A=
ENST00000525803.1:c.61A=	ENSP00000431750.1:p.Ser21=
ENST00000528679.5:c.61A=	ENSP00000435895.1:p.Ser21=
ENST00000531673.5:c.61A=	ENSP00000433469.1:p.Ser21=
NM_000317.2:c.61A=	NP_000308.1:p.Ser21=
NM_000317.3:c.61A= MANE Select	NP_000308.1:p.Ser21=