Canonical Allele Identifier: CA476797414

Gene: PTS

Linked Data

• MyVariant Identifiers: chr11:g.112100944A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112230221A>T , CM000673.2:g.112230221A>T	GRCh38
NC_000011.9:g.112100944A>T , CM000673.1:g.112100944A>T	GRCh37
NC_000011.8:g.111606154A>T	NCBI36
NG_008743.1:g.8857A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.177A>T MANE Select	ENSP00000280362.3:p.Val59=
ENST00000280362.7:c.177A>T	ENSP00000280362.3:p.Val59=
ENST00000524931.1:c.-28A>T	ENSP00000434688.1:n.-28A>T
ENST00000525803.1:c.163+1548A>T	ENSP00000431750.1:n.163+1548A>T
ENST00000528679.5:c.164-405A>T	ENSP00000435895.1:n.164-405A>T
ENST00000531175.1:n.128A>T
ENST00000531673.5:c.164-405A>T	ENSP00000433469.1:n.164-405A>T
NM_000317.2:c.177A>T	NP_000308.1:p.Val59=
XM_011542943.1:c.138A>T	XP_011541245.1:p.Val46=
NM_000317.3:c.177A>T MANE Select	NP_000308.1:p.Val59=