Canonical Allele Identifier: CA9471493
Gene: ERF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.42250456G>A , CM000681.2:g.42250456G>A GRCh38
NC_000019.9:g.42754608G>A , CM000681.1:g.42754608G>A GRCh37
NC_000019.8:g.47446448G>A NCBI36
NG_042802.1:g.9709C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222329.9:c.132C>T MANE Select ENSP00000222329.3:p.Gly44=
ENST00000222329.8:c.132C>T ENSP00000222329.3:p.Gly44=
ENST00000440177.6:c.-94C>T ENSP00000388173.2:n.-94C>T
ENST00000593944.5:c.-94C>T ENSP00000469274.1:n.-94C>T
ENST00000594664.1:c.22+4522C>T ENSP00000470087.1:n.22+4522C>T
ENST00000595941.1:n.215C>T
ENST00000596818.1:n.240C>T
NM_001301035.1:c.-94C>T NP_001287964.1:n.-94C>T
NM_001308402.1:c.-94C>T NP_001295331.1:n.-94C>T
NM_001312656.1:c.-94C>T NP_001299585.1:n.-94C>T
NM_006494.3:c.132C>T NP_006485.2:p.Gly44=
XM_011526612.1:c.-94C>T XP_011524914.1:n.-94C>T
XM_011526613.1:c.-94C>T XP_011524915.1:n.-94C>T
XM_017026468.1:c.-94C>T XP_016881957.1:n.-94C>T
XM_017026469.1:c.-94C>T XP_016881958.1:n.-94C>T
NM_006494.4:c.132C>T MANE Select NP_006485.2:p.Gly44=
NM_001308402.2:c.-94C>T NP_001295331.1:n.-94C>T
NM_001312656.2:c.-94C>T NP_001299585.1:n.-94C>T
NM_001301035.2:c.-94C>T NP_001287964.1:n.-94C>T