Canonical Allele Identifier: CA406114260

Gene: ERF

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.42249845T>G , CM000681.2:g.42249845T>G	GRCh38
NC_000019.9:g.42753997T>G , CM000681.1:g.42753997T>G	GRCh37
NC_000019.8:g.47445837T>G	NCBI36
NG_042802.1:g.10320A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222329.9:c.355A>C MANE Select	ENSP00000222329.3:p.Ile119Leu
ENST00000222329.8:c.355A>C	ENSP00000222329.3:p.Ile119Leu
ENST00000440177.6:c.130A>C	ENSP00000388173.2:p.Ile44Leu
ENST00000593944.5:c.130A>C	ENSP00000469274.1:p.Ile44Leu
ENST00000594664.1:c.22+5133A>C	ENSP00000470087.1:n.22+5133A>C
ENST00000595448.1:n.328A>C
ENST00000598965.1:c.130A>C	ENSP00000468962.1:p.Ile44Leu
NM_001301035.1:c.130A>C	NP_001287964.1:p.Ile44Leu
NM_001308402.1:c.130A>C	NP_001295331.1:p.Ile44Leu
NM_001312656.1:c.130A>C	NP_001299585.1:p.Ile44Leu
NM_006494.3:c.355A>C	NP_006485.2:p.Ile119Leu
XM_011526612.1:c.130A>C	XP_011524914.1:p.Ile44Leu
XM_011526613.1:c.130A>C	XP_011524915.1:p.Ile44Leu
XM_017026468.1:c.130A>C	XP_016881957.1:p.Ile44Leu
XM_017026469.1:c.130A>C	XP_016881958.1:p.Ile44Leu
NM_006494.4:c.355A>C MANE Select	NP_006485.2:p.Ile119Leu
NM_001308402.2:c.130A>C	NP_001295331.1:p.Ile44Leu
NM_001312656.2:c.130A>C	NP_001299585.1:p.Ile44Leu
NM_001301035.2:c.130A>C	NP_001287964.1:p.Ile44Leu