Canonical Allele Identifier: CA659978416

Gene: GPAM

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.112174128A>T , CM000672.2:g.112174128A>T	GRCh38
NC_000010.10:g.113933886A>T , CM000672.1:g.113933886A>T	GRCh37
NC_000010.9:g.113923876A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348367.9:c.414-283T>A MANE Select	ENSP00000265276.4:n.414-283T>A
ENST00000348367.8:c.414-283T>A	ENSP00000265276.4:n.414-283T>A
ENST00000369425.5:c.414-283T>A	ENSP00000358433.1:n.414-283T>A
NM_001244949.1:c.414-283T>A	NP_001231878.1:n.414-283T>A
NM_020918.5:c.414-283T>A	NP_065969.3:n.414-283T>A
XM_005269998.1:c.414-283T>A	XP_005270055.1:n.414-283T>A
XM_024448089.1:c.414-283T>A	XP_024303857.1:n.414-283T>A
NM_001244949.2:c.414-283T>A MANE Select	NP_001231878.1:n.414-283T>A
NM_020918.6:c.414-283T>A	NP_065969.3:n.414-283T>A