Canonical Allele Identifier: CA2748872152

Gene: GREB1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11587736_11587737insCC , CM000664.2:g.11587736_11587737insCC	GRCh38
NC_000002.11:g.11727862_11727863insCC , CM000664.1:g.11727862_11727863insCC	GRCh37
NC_000002.10:g.11645313_11645314insCC	NCBI36
NG_029429.1:g.58621_58622insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381486.7:c.1160-1010_1160-1009insCC MANE Select	ENSP00000370896.2:n.1160-1010_1160-1009insCC
ENST00000234142.9:c.1160-1010_1160-1009insCC	ENSP00000234142.5:n.1160-1010_1160-1009insCC
ENST00000263834.9:c.*284_*285insCC	ENSP00000263834.5:n.*284_*285insCC
ENST00000381483.6:c.1160-1010_1160-1009insCC	ENSP00000370892.2:n.1160-1010_1160-1009insCC
ENST00000381486.6:c.1160-1010_1160-1009insCC	ENSP00000370896.2:n.1160-1010_1160-1009insCC
NM_014668.3:c.1160-1010_1160-1009insCC	NP_055483.2:n.1160-1010_1160-1009insCC
NM_033090.2:c.1160-1010_1160-1009insCC	NP_149081.1:n.1160-1010_1160-1009insCC
NM_148903.2:c.*284_*285insCC	NP_683701.2:n.*284_*285insCC
XM_005246192.3:c.1160-1010_1160-1009insCC	XP_005246249.1:n.1160-1010_1160-1009insCC
XM_011510418.1:c.1160-1010_1160-1009insCC	XP_011508720.1:n.1160-1010_1160-1009insCC
XM_011510419.1:c.1160-1010_1160-1009insCC	XP_011508721.1:n.1160-1010_1160-1009insCC
XM_011510420.1:c.1160-1010_1160-1009insCC	XP_011508722.1:n.1160-1010_1160-1009insCC
XM_011510421.1:c.1160-1010_1160-1009insCC	XP_011508723.1:n.1160-1010_1160-1009insCC
XM_011510423.1:c.1160-1010_1160-1009insCC	XP_011508725.1:n.1160-1010_1160-1009insCC
XR_922686.1:n.1321-1010_1321-1009insCC
XM_005246192.4:c.1160-1010_1160-1009insCC	XP_005246249.1:n.1160-1010_1160-1009insCC
XM_011510418.3:c.1160-1010_1160-1009insCC	XP_011508720.1:n.1160-1010_1160-1009insCC
XM_011510419.3:c.1160-1010_1160-1009insCC	XP_011508721.1:n.1160-1010_1160-1009insCC
XM_011510423.3:c.1160-1010_1160-1009insCC	XP_011508725.1:n.1160-1010_1160-1009insCC
XM_024453250.1:c.1160-1010_1160-1009insCC	XP_024309018.1:n.1160-1010_1160-1009insCC
XM_024453251.1:c.1160-1010_1160-1009insCC	XP_024309019.1:n.1160-1010_1160-1009insCC
XM_024453252.1:c.1160-1010_1160-1009insCC	XP_024309020.1:n.1160-1010_1160-1009insCC
XM_024453253.1:c.1160-1010_1160-1009insCC	XP_024309021.1:n.1160-1010_1160-1009insCC
XM_024453254.1:c.1160-1010_1160-1009insCC	XP_024309022.1:n.1160-1010_1160-1009insCC
XM_024453255.1:c.1160-1010_1160-1009insCC	XP_024309023.1:n.1160-1010_1160-1009insCC
XM_024453256.1:c.1160-1010_1160-1009insCC	XP_024309024.1:n.1160-1010_1160-1009insCC
XR_001739081.2:n.2090-1010_2090-1009insCC
XR_922686.3:n.2089-1010_2089-1009insCC
NM_014668.4:c.1160-1010_1160-1009insCC MANE Select	NP_055483.2:n.1160-1010_1160-1009insCC
NM_033090.3:c.1160-1010_1160-1009insCC	NP_149081.1:n.1160-1010_1160-1009insCC
NM_148903.3:c.*284_*285insCC	NP_683701.2:n.*284_*285insCC