Canonical Allele Identifier: CA382627526

Gene: PTS

Linked Data

• MyVariant Identifiers: chr11:g.112100937T>G (hg19) ; chr11:g.112230214T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112230214T>G , CM000673.2:g.112230214T>G	GRCh38
NC_000011.9:g.112100937T>G , CM000673.1:g.112100937T>G	GRCh37
NC_000011.8:g.111606147T>G	NCBI36
NG_008743.1:g.8850T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.170T>G MANE Select	ENSP00000280362.3:p.Val57Gly
ENST00000280362.7:c.170T>G	ENSP00000280362.3:p.Val57Gly
ENST00000524931.1:c.-35T>G	ENSP00000434688.1:n.-35T>G
ENST00000525803.1:c.163+1541T>G	ENSP00000431750.1:n.163+1541T>G
ENST00000528679.5:c.164-412T>G	ENSP00000435895.1:n.164-412T>G
ENST00000531175.1:n.121T>G
ENST00000531673.5:c.164-412T>G	ENSP00000433469.1:n.164-412T>G
NM_000317.2:c.170T>G	NP_000308.1:p.Val57Gly
XM_011542943.1:c.131T>G	XP_011541245.1:p.Val44Gly
NM_000317.3:c.170T>G MANE Select	NP_000308.1:p.Val57Gly