Canonical Allele Identifier: CA406105029

Gene: ERF

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.42248695C>G , CM000681.2:g.42248695C>G	GRCh38
NC_000019.9:g.42752847C>G , CM000681.1:g.42752847C>G	GRCh37
NC_000019.8:g.47444687C>G	NCBI36
NG_042802.1:g.11470G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006494.4:c.1417G>C MANE Select	NP_006485.2:p.Gly473Arg
ENST00000222329.9:c.1417G>C MANE Select	ENSP00000222329.3:p.Gly473Arg
NM_001301035.1:c.1192G>C	NP_001287964.1:p.Gly398Arg
NM_001301035.2:c.1192G>C	NP_001287964.1:p.Gly398Arg
NM_001308402.1:c.1192G>C	NP_001295331.1:p.Gly398Arg
NM_001308402.2:c.1192G>C	NP_001295331.1:p.Gly398Arg
NM_001312656.1:c.1192G>C	NP_001299585.1:p.Gly398Arg
NM_001312656.2:c.1192G>C	NP_001299585.1:p.Gly398Arg
NM_006494.3:c.1417G>C	NP_006485.2:p.Gly473Arg
ENST00000222329.8:c.1417G>C	ENSP00000222329.3:p.Gly473Arg
ENST00000440177.6:c.1192G>C	ENSP00000388173.2:p.Gly398Arg
ENST00000594664.1:c.22+6283G>C	ENSP00000470087.1:n.22+6283G>C
XM_011526612.1:c.1192G>C	XP_011524914.1:p.Gly398Arg
XM_011526613.1:c.1192G>C	XP_011524915.1:p.Gly398Arg
XM_017026468.1:c.1192G>C	XP_016881957.1:p.Gly398Arg
XM_017026469.1:c.1192G>C	XP_016881958.1:p.Gly398Arg