Canonical Allele Identifier: CA916474212

Gene: GREB1

Linked Data

• dbSNP Id: rs1572830313
• gnomAD v3: 2-11587712-C-CAT
• gnomAD v4: 2-11587712-C-CAT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11587713_11587714insTA , CM000664.2:g.11587713_11587714insTA	GRCh38
NC_000002.11:g.11727839_11727840insTA , CM000664.1:g.11727839_11727840insTA	GRCh37
NC_000002.10:g.11645290_11645291insTA	NCBI36
NG_029429.1:g.58598_58599insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381486.7:c.1160-1033_1160-1032insTA MANE Select	ENSP00000370896.2:n.1160-1033_1160-1032insTA
ENST00000234142.9:c.1160-1033_1160-1032insTA	ENSP00000234142.5:n.1160-1033_1160-1032insTA
ENST00000263834.9:c.*261_*262insTA	ENSP00000263834.5:n.*261_*262insTA
ENST00000381483.6:c.1160-1033_1160-1032insTA	ENSP00000370892.2:n.1160-1033_1160-1032insTA
ENST00000381486.6:c.1160-1033_1160-1032insTA	ENSP00000370896.2:n.1160-1033_1160-1032insTA
NM_014668.3:c.1160-1033_1160-1032insTA	NP_055483.2:n.1160-1033_1160-1032insTA
NM_033090.2:c.1160-1033_1160-1032insTA	NP_149081.1:n.1160-1033_1160-1032insTA
NM_148903.2:c.*261_*262insTA	NP_683701.2:n.*261_*262insTA
XM_005246192.3:c.1160-1033_1160-1032insTA	XP_005246249.1:n.1160-1033_1160-1032insTA
XM_011510418.1:c.1160-1033_1160-1032insTA	XP_011508720.1:n.1160-1033_1160-1032insTA
XM_011510419.1:c.1160-1033_1160-1032insTA	XP_011508721.1:n.1160-1033_1160-1032insTA
XM_011510420.1:c.1160-1033_1160-1032insTA	XP_011508722.1:n.1160-1033_1160-1032insTA
XM_011510421.1:c.1160-1033_1160-1032insTA	XP_011508723.1:n.1160-1033_1160-1032insTA
XM_011510423.1:c.1160-1033_1160-1032insTA	XP_011508725.1:n.1160-1033_1160-1032insTA
XR_922686.1:n.1321-1033_1321-1032insTA
XM_005246192.4:c.1160-1033_1160-1032insTA	XP_005246249.1:n.1160-1033_1160-1032insTA
XM_011510418.3:c.1160-1033_1160-1032insTA	XP_011508720.1:n.1160-1033_1160-1032insTA
XM_011510419.3:c.1160-1033_1160-1032insTA	XP_011508721.1:n.1160-1033_1160-1032insTA
XM_011510423.3:c.1160-1033_1160-1032insTA	XP_011508725.1:n.1160-1033_1160-1032insTA
XM_024453250.1:c.1160-1033_1160-1032insTA	XP_024309018.1:n.1160-1033_1160-1032insTA
XM_024453251.1:c.1160-1033_1160-1032insTA	XP_024309019.1:n.1160-1033_1160-1032insTA
XM_024453252.1:c.1160-1033_1160-1032insTA	XP_024309020.1:n.1160-1033_1160-1032insTA
XM_024453253.1:c.1160-1033_1160-1032insTA	XP_024309021.1:n.1160-1033_1160-1032insTA
XM_024453254.1:c.1160-1033_1160-1032insTA	XP_024309022.1:n.1160-1033_1160-1032insTA
XM_024453255.1:c.1160-1033_1160-1032insTA	XP_024309023.1:n.1160-1033_1160-1032insTA
XM_024453256.1:c.1160-1033_1160-1032insTA	XP_024309024.1:n.1160-1033_1160-1032insTA
XR_001739081.2:n.2090-1033_2090-1032insTA
XR_922686.3:n.2089-1033_2089-1032insTA
NM_014668.4:c.1160-1033_1160-1032insTA MANE Select	NP_055483.2:n.1160-1033_1160-1032insTA
NM_033090.3:c.1160-1033_1160-1032insTA	NP_149081.1:n.1160-1033_1160-1032insTA
NM_148903.3:c.*261_*262insTA	NP_683701.2:n.*261_*262insTA