Canonical Allele Identifier: CA296943778

Gene: GREB1L

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.21496478G>A , CM000680.2:g.21496478G>A	GRCh38
NC_000018.9:g.19076439G>A , CM000680.1:g.19076439G>A	GRCh37
NC_000018.8:g.17330437G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001142966.3:c.3171G>A MANE Select	NP_001136438.1:p.Arg1057=
ENST00000424526.7:c.3171G>A MANE Select	ENSP00000412060.1:p.Arg1057=
NM_001142966.1:c.3171G>A	NP_001136438.1:p.Arg1057=
NM_001142966.2:c.3171G>A	NP_001136438.1:p.Arg1057=
ENST00000269218.10:c.2844G>A	ENSP00000269218.6:p.Arg948=
ENST00000424526.5:c.3171G>A	ENSP00000412060.1:p.Arg1057=
ENST00000424526.6:c.3171G>A	ENSP00000412060.1:p.Arg1057=
ENST00000578955.1:n.1194G>A
ENST00000579454.2:c.3300G>A	ENSP00000463926.2:p.Arg1100=
ENST00000580732.6:c.3171G>A	ENSP00000464162.1:p.Arg1057=
XM_006722547.1:c.3300G>A	XP_006722610.1:p.Arg1100=
XM_006722547.3:c.3300G>A	XP_006722610.1:p.Arg1100=
XM_011526176.1:c.3300G>A	XP_011524478.1:p.Arg1100=
XM_011526177.1:c.3300G>A	XP_011524479.1:p.Arg1100=
XM_011526178.1:c.3171G>A	XP_011524480.1:p.Arg1057=
XM_011526179.1:c.3300G>A	XP_011524481.1:p.Arg1100=
XM_011526179.3:c.3300G>A	XP_011524481.1:p.Arg1100=
XM_011526180.1:c.2973G>A	XP_011524482.1:p.Arg991=
XM_011526181.1:c.2844G>A	XP_011524483.1:p.Arg948=
XM_011526182.1:c.462G>A	XP_011524484.1:p.Arg154=
XM_017025988.1:c.3300G>A	XP_016881477.1:p.Arg1100=
XM_017025989.1:c.3300G>A	XP_016881478.1:p.Arg1100=
XM_017025990.1:c.3300G>A	XP_016881479.1:p.Arg1100=
XM_017025991.1:c.3216G>A	XP_016881480.1:p.Arg1072=
XM_017025992.1:c.3171G>A	XP_016881481.1:p.Arg1057=
XM_017025993.1:c.3171G>A	XP_016881482.1:p.Arg1057=
XM_017025994.1:c.2973G>A	XP_016881483.1:p.Arg991=
XM_017025995.1:c.2889G>A	XP_016881484.1:p.Arg963=
XM_017025996.1:c.2844G>A	XP_016881485.1:p.Arg948=