Canonical Allele Identifier: CA397786487

Gene: GPS2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7314078A>C , CM000679.2:g.7314078A>C	GRCh38
NC_000017.10:g.7217397A>C , CM000679.1:g.7217397A>C	GRCh37
NC_000017.9:g.7158121A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380728.7:c.397+2T>G MANE Select	ENSP00000370104.2:n.397+2T>G
ENST00000315601.8:c.1667+2T>G
ENST00000380728.6:c.397+2T>G	ENSP00000370104.2:n.397+2T>G
ENST00000389167.9:c.397+2T>G	ENSP00000379841.4:n.397+2T>G
ENST00000570780.5:c.468+2T>G
ENST00000571098.5:n.631+2T>G
ENST00000571569.5:n.902+2T>G
ENST00000571695.1:n.526T>G
ENST00000571697.5:n.1059+2T>G
ENST00000572172.5:n.666+2T>G
ENST00000572363.5:n.543T>G
ENST00000572707.5:n.826+2T>G
ENST00000573059.5:n.506+2T>G
ENST00000575474.1:c.1889+2T>G
ENST00000577040.2:c.397+2T>G	ENSP00000461624.2:n.397+2T>G
NM_004489.4:c.397+2T>G	NP_004480.1:n.397+2T>G
NM_004489.5:c.397+2T>G MANE Select	NP_004480.1:n.397+2T>G