Canonical Allele Identifier: CA406103840

Gene: ERF

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.42248550G>C , CM000681.2:g.42248550G>C	GRCh38
NC_000019.9:g.42752702G>C , CM000681.1:g.42752702G>C	GRCh37
NC_000019.8:g.47444542G>C	NCBI36
NG_042802.1:g.11615C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006494.4:c.1562C>G MANE Select	NP_006485.2:p.Ala521Gly
ENST00000222329.9:c.1562C>G MANE Select	ENSP00000222329.3:p.Ala521Gly
NM_001301035.1:c.1337C>G	NP_001287964.1:p.Ala446Gly
NM_001301035.2:c.1337C>G	NP_001287964.1:p.Ala446Gly
NM_001308402.1:c.1337C>G	NP_001295331.1:p.Ala446Gly
NM_001308402.2:c.1337C>G	NP_001295331.1:p.Ala446Gly
NM_001312656.1:c.1337C>G	NP_001299585.1:p.Ala446Gly
NM_001312656.2:c.1337C>G	NP_001299585.1:p.Ala446Gly
NM_006494.3:c.1562C>G	NP_006485.2:p.Ala521Gly
ENST00000222329.8:c.1562C>G	ENSP00000222329.3:p.Ala521Gly
ENST00000440177.6:c.1337C>G	ENSP00000388173.2:p.Ala446Gly
ENST00000594664.1:c.22+6428C>G	ENSP00000470087.1:n.22+6428C>G
ENST00000676949.1:n.30+40C>G
XM_011526612.1:c.1337C>G	XP_011524914.1:p.Ala446Gly
XM_011526613.1:c.1337C>G	XP_011524915.1:p.Ala446Gly
XM_017026468.1:c.1337C>G	XP_016881957.1:p.Ala446Gly
XM_017026469.1:c.1337C>G	XP_016881958.1:p.Ala446Gly