Canonical Allele Identifier: CA2574980265

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112228683A>G , CM000673.2:g.112228683A>G	GRCh38
NC_000011.9:g.112099406A>G , CM000673.1:g.112099406A>G	GRCh37
NC_000011.8:g.111604616A>G	NCBI36
NG_008743.1:g.7319A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000280362.8:c.163+10A>G MANE Select	ENSP00000280362.3:n.163+10A>G
ENST00000280362.7:c.163+10A>G	ENSP00000280362.3:n.163+10A>G
ENST00000524931.1:c.-42+10A>G	ENSP00000434688.1:n.-42+10A>G
ENST00000525645.1:n.248A>G
ENST00000525803.1:c.163+10A>G	ENSP00000431750.1:n.163+10A>G
ENST00000528679.5:c.163+10A>G	ENSP00000435895.1:n.163+10A>G
ENST00000531673.5:c.163+10A>G	ENSP00000433469.1:n.163+10A>G
NM_000317.2:c.163+10A>G	NP_000308.1:n.163+10A>G
XM_011542943.1:c.-680A>G	XP_011541245.1:n.-680A>G
NM_000317.3:c.163+10A>G MANE Select	NP_000308.1:n.163+10A>G