Canonical Allele Identifier: CA1531046

Gene: GREB1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11556652G>A , CM000664.2:g.11556652G>A	GRCh38
NC_000002.11:g.11696778G>A , CM000664.1:g.11696778G>A	GRCh37
NC_000002.10:g.11614229G>A	NCBI36
NG_029429.1:g.27537G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014668.4:c.38G>A MANE Select	NP_055483.2:p.Arg13His
ENST00000381486.7:c.38G>A MANE Select	ENSP00000370896.2:p.Arg13His
NM_014668.3:c.38G>A	NP_055483.2:p.Arg13His
NM_033090.2:c.38G>A	NP_149081.1:p.Arg13His
NM_033090.3:c.38G>A	NP_149081.1:p.Arg13His
NM_148903.2:c.38G>A	NP_683701.2:p.Arg13His
NM_148903.3:c.38G>A	NP_683701.2:p.Arg13His
ENST00000234142.9:c.38G>A	ENSP00000234142.5:p.Arg13His
ENST00000263834.9:c.38G>A	ENSP00000263834.5:p.Arg13His
ENST00000381483.6:c.38G>A	ENSP00000370892.2:p.Arg13His
ENST00000381486.6:c.38G>A	ENSP00000370896.2:p.Arg13His
ENST00000389825.7:c.-173-5811G>A	ENSP00000374475.3:n.-173-5811G>A
ENST00000470980.1:n.35G>A
ENST00000628795.2:c.38G>A	ENSP00000487278.1:p.Arg13His
XM_005246192.3:c.38G>A	XP_005246249.1:p.Arg13His
XM_005246192.4:c.38G>A	XP_005246249.1:p.Arg13His
XM_011510418.1:c.38G>A	XP_011508720.1:p.Arg13His
XM_011510418.3:c.38G>A	XP_011508720.1:p.Arg13His
XM_011510419.1:c.38G>A	XP_011508721.1:p.Arg13His
XM_011510419.3:c.38G>A	XP_011508721.1:p.Arg13His
XM_011510420.1:c.38G>A	XP_011508722.1:p.Arg13His
XM_011510421.1:c.38G>A	XP_011508723.1:p.Arg13His
XM_011510423.1:c.38G>A	XP_011508725.1:p.Arg13His
XM_011510423.3:c.38G>A	XP_011508725.1:p.Arg13His
XM_024453250.1:c.38G>A	XP_024309018.1:p.Arg13His
XM_024453251.1:c.38G>A	XP_024309019.1:p.Arg13His
XM_024453252.1:c.38G>A	XP_024309020.1:p.Arg13His
XM_024453253.1:c.38G>A	XP_024309021.1:p.Arg13His
XM_024453254.1:c.38G>A	XP_024309022.1:p.Arg13His
XM_024453255.1:c.38G>A	XP_024309023.1:p.Arg13His
XM_024453256.1:c.38G>A	XP_024309024.1:p.Arg13His
XR_001739081.2:n.968G>A
XR_922686.1:n.199G>A
XR_922686.3:n.967G>A