Canonical Allele Identifier: CA2614931257

Gene: FOLR2

Linked Data

• gnomAD v4: 11-72218395-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72218397del , CM000673.2:g.72218397del	GRCh38
NC_000011.9:g.71929441del , CM000673.1:g.71929441del	GRCh37
NC_000011.8:g.71607089del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298223.11:c.-24-164del MANE Select	ENSP00000298223.6:n.-24-164del
ENST00000298223.10:c.-24-164del	ENSP00000298223.6:n.-24-164del
ENST00000321324.11:c.28-176del	ENSP00000321957.7:n.28-176del
ENST00000449475.6:c.28-164del	ENSP00000405638.2:n.28-164del
ENST00000454954.6:c.27+1472del	ENSP00000414094.2:n.27+1472del
ENST00000535625.5:c.-24-164del	ENSP00000444794.1:n.-24-164del
ENST00000536778.5:c.22-164del	ENSP00000438568.1:n.22-164del
ENST00000539412.5:c.22-176del	ENSP00000441547.1:n.22-176del
ENST00000541003.5:c.115-164del	ENSP00000443307.1:n.115-164del
ENST00000619261.4:c.28-164del	ENSP00000480592.1:n.28-164del
NM_000803.4:c.-24-164del	NP_000794.3:n.-24-164del
NM_001113534.1:c.-24-164del	NP_001107006.1:n.-24-164del
NM_001113535.1:c.-12-176del	NP_001107007.1:n.-12-176del
NM_001113536.1:c.-12-176del	NP_001107008.1:n.-12-176del
XM_005273856.2:c.4-164del	XP_005273913.1:n.4-164del
XM_011544869.1:c.28-164del	XP_011543171.1:n.28-164del
XM_011544870.1:c.22-164del	XP_011543172.1:n.22-164del
XM_011544871.1:c.28-176del	XP_011543173.1:n.28-176del
XM_011544872.1:c.22-176del	XP_011543174.1:n.22-176del
XM_005273856.4:c.4-164del	XP_005273913.1:n.4-164del
XM_024448412.1:c.28-164del	XP_024304180.1:n.28-164del
NM_000803.5:c.-24-164del MANE Select	NP_000794.3:n.-24-164del
NM_001113534.2:c.-24-164del	NP_001107006.1:n.-24-164del
NM_001113535.2:c.-12-176del	NP_001107007.1:n.-12-176del
NM_001113536.2:c.-12-176del	NP_001107008.1:n.-12-176del