Canonical Allele Identifier: CA308638312

Gene: ERF

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.42249915G>A , CM000681.2:g.42249915G>A	GRCh38
NC_000019.9:g.42754067G>A , CM000681.1:g.42754067G>A	GRCh37
NC_000019.8:g.47445907G>A	NCBI36
NG_042802.1:g.10250C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222329.9:c.285C>T MANE Select	ENSP00000222329.3:p.His95=
ENST00000222329.8:c.285C>T	ENSP00000222329.3:p.His95=
ENST00000440177.6:c.60C>T	ENSP00000388173.2:p.His20=
ENST00000593944.5:c.60C>T	ENSP00000469274.1:p.His20=
ENST00000594664.1:c.22+5063C>T	ENSP00000470087.1:n.22+5063C>T
ENST00000595448.1:n.258C>T
ENST00000598965.1:c.60C>T	ENSP00000468962.1:p.His20=
NM_001301035.1:c.60C>T	NP_001287964.1:p.His20=
NM_001308402.1:c.60C>T	NP_001295331.1:p.His20=
NM_001312656.1:c.60C>T	NP_001299585.1:p.His20=
NM_006494.3:c.285C>T	NP_006485.2:p.His95=
XM_011526612.1:c.60C>T	XP_011524914.1:p.His20=
XM_011526613.1:c.60C>T	XP_011524915.1:p.His20=
XM_017026468.1:c.60C>T	XP_016881957.1:p.His20=
XM_017026469.1:c.60C>T	XP_016881958.1:p.His20=
NM_006494.4:c.285C>T MANE Select	NP_006485.2:p.His95=
NM_001308402.2:c.60C>T	NP_001295331.1:p.His20=
NM_001312656.2:c.60C>T	NP_001299585.1:p.His20=
NM_001301035.2:c.60C>T	NP_001287964.1:p.His20=