Canonical Allele Identifier: CA381743218

Gene: FOLR2

Linked Data

• MyVariant Identifiers: chr11:g.71929614C>A (hg19) ; chr11:g.72218570C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72218570C>A , CM000673.2:g.72218570C>A	GRCh38
NC_000011.9:g.71929614C>A , CM000673.1:g.71929614C>A	GRCh37
NC_000011.8:g.71607262C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298223.11:c.-15C>A MANE Select	ENSP00000298223.6:n.-15C>A
ENST00000298223.10:c.-15C>A	ENSP00000298223.6:n.-15C>A
ENST00000321324.11:c.28-3C>A	ENSP00000321957.7:n.28-3C>A
ENST00000449475.6:c.37C>A	ENSP00000405638.2:p.Gln13Lys
ENST00000454954.6:c.27+1645C>A	ENSP00000414094.2:n.27+1645C>A
ENST00000535625.5:c.-15C>A	ENSP00000444794.1:n.-15C>A
ENST00000536778.5:c.31C>A	ENSP00000438568.1:p.Gln11Lys
ENST00000538353.1:c.-15C>A	ENSP00000440337.1:n.-15C>A
ENST00000539412.5:c.22-3C>A	ENSP00000441547.1:n.22-3C>A
ENST00000541003.5:c.124C>A	ENSP00000443307.1:p.Gln42Lys
ENST00000619261.4:c.37C>A	ENSP00000480592.1:p.Gln13Lys
NM_000803.4:c.-15C>A	NP_000794.3:n.-15C>A
NM_001113534.1:c.-15C>A	NP_001107006.1:n.-15C>A
NM_001113535.1:c.-12-3C>A	NP_001107007.1:n.-12-3C>A
NM_001113536.1:c.-12-3C>A	NP_001107008.1:n.-12-3C>A
XM_005273856.2:c.13C>A	XP_005273913.1:p.Gln5Lys
XM_011544869.1:c.37C>A	XP_011543171.1:p.Gln13Lys
XM_011544870.1:c.31C>A	XP_011543172.1:p.Gln11Lys
XM_011544871.1:c.28-3C>A	XP_011543173.1:n.28-3C>A
XM_011544872.1:c.22-3C>A	XP_011543174.1:n.22-3C>A
XM_005273856.4:c.13C>A	XP_005273913.1:p.Gln5Lys
XM_024448412.1:c.37C>A	XP_024304180.1:p.Gln13Lys
NM_000803.5:c.-15C>A MANE Select	NP_000794.3:n.-15C>A
NM_001113534.2:c.-15C>A	NP_001107006.1:n.-15C>A
NM_001113535.2:c.-12-3C>A	NP_001107007.1:n.-12-3C>A
NM_001113536.2:c.-12-3C>A	NP_001107008.1:n.-12-3C>A