Canonical Allele Identifier: CA475605869

Gene: FOLR2

Linked Data

• MyVariant Identifiers: chr11:g.71929649A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72218605A>T , CM000673.2:g.72218605A>T	GRCh38
NC_000011.9:g.71929649A>T , CM000673.1:g.71929649A>T	GRCh37
NC_000011.8:g.71607297A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298223.11:c.21A>T MANE Select	ENSP00000298223.6:p.Pro7=
ENST00000298223.10:c.21A>T	ENSP00000298223.6:p.Pro7=
ENST00000321324.11:c.60A>T	ENSP00000321957.7:p.Pro20=
ENST00000449475.6:c.72A>T	ENSP00000405638.2:p.Pro24=
ENST00000454954.6:c.27+1680A>T	ENSP00000414094.2:n.27+1680A>T
ENST00000535625.5:c.21A>T	ENSP00000444794.1:p.Pro7=
ENST00000536778.5:c.66A>T	ENSP00000438568.1:p.Pro22=
ENST00000538353.1:c.21A>T	ENSP00000440337.1:p.Pro7=
ENST00000539412.5:c.54A>T	ENSP00000441547.1:p.Pro18=
ENST00000541003.5:c.159A>T	ENSP00000443307.1:p.Pro53=
ENST00000619261.4:c.72A>T	ENSP00000480592.1:p.Pro24=
NM_000803.4:c.21A>T	NP_000794.3:p.Pro7=
NM_001113534.1:c.21A>T	NP_001107006.1:p.Pro7=
NM_001113535.1:c.21A>T	NP_001107007.1:p.Pro7=
NM_001113536.1:c.21A>T	NP_001107008.1:p.Pro7=
XM_005273856.2:c.48A>T	XP_005273913.1:p.Pro16=
XM_011544869.1:c.72A>T	XP_011543171.1:p.Pro24=
XM_011544870.1:c.66A>T	XP_011543172.1:p.Pro22=
XM_011544871.1:c.60A>T	XP_011543173.1:p.Pro20=
XM_011544872.1:c.54A>T	XP_011543174.1:p.Pro18=
XM_005273856.4:c.48A>T	XP_005273913.1:p.Pro16=
XM_024448412.1:c.72A>T	XP_024304180.1:p.Pro24=
NM_000803.5:c.21A>T MANE Select	NP_000794.3:p.Pro7=
NM_001113534.2:c.21A>T	NP_001107006.1:p.Pro7=
NM_001113535.2:c.21A>T	NP_001107007.1:p.Pro7=
NM_001113536.2:c.21A>T	NP_001107008.1:p.Pro7=