Canonical Allele Identifier: CA916474238
Gene: GREB1 HGNC NCBI

Linked Data

dbSNP Id: rs1553366381

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11587743_11587744dup , CM000664.2:g.11587743_11587744dup GRCh38
NC_000002.11:g.11727869_11727870dup , CM000664.1:g.11727869_11727870dup GRCh37
NC_000002.10:g.11645320_11645321dup NCBI36
NG_029429.1:g.58628_58629dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000381486.7:c.1160-1003_1160-1002dup MANE Select ENSP00000370896.2:n.1160-1003_1160-1002dup
ENST00000234142.9:c.1160-1003_1160-1002dup ENSP00000234142.5:n.1160-1003_1160-1002dup
ENST00000263834.9:c.*291_*292dup ENSP00000263834.5:n.*291_*292dup
ENST00000381483.6:c.1160-1003_1160-1002dup ENSP00000370892.2:n.1160-1003_1160-1002dup
ENST00000381486.6:c.1160-1003_1160-1002dup ENSP00000370896.2:n.1160-1003_1160-1002dup
NM_014668.3:c.1160-1003_1160-1002dup NP_055483.2:n.1160-1003_1160-1002dup
NM_033090.2:c.1160-1003_1160-1002dup NP_149081.1:n.1160-1003_1160-1002dup
NM_148903.2:c.*291_*292dup NP_683701.2:n.*291_*292dup
XM_005246192.3:c.1160-1003_1160-1002dup XP_005246249.1:n.1160-1003_1160-1002dup
XM_011510418.1:c.1160-1003_1160-1002dup XP_011508720.1:n.1160-1003_1160-1002dup
XM_011510419.1:c.1160-1003_1160-1002dup XP_011508721.1:n.1160-1003_1160-1002dup
XM_011510420.1:c.1160-1003_1160-1002dup XP_011508722.1:n.1160-1003_1160-1002dup
XM_011510421.1:c.1160-1003_1160-1002dup XP_011508723.1:n.1160-1003_1160-1002dup
XM_011510423.1:c.1160-1003_1160-1002dup XP_011508725.1:n.1160-1003_1160-1002dup
XR_922686.1:n.1321-1003_1321-1002dup
XM_005246192.4:c.1160-1003_1160-1002dup XP_005246249.1:n.1160-1003_1160-1002dup
XM_011510418.3:c.1160-1003_1160-1002dup XP_011508720.1:n.1160-1003_1160-1002dup
XM_011510419.3:c.1160-1003_1160-1002dup XP_011508721.1:n.1160-1003_1160-1002dup
XM_011510423.3:c.1160-1003_1160-1002dup XP_011508725.1:n.1160-1003_1160-1002dup
XM_024453250.1:c.1160-1003_1160-1002dup XP_024309018.1:n.1160-1003_1160-1002dup
XM_024453251.1:c.1160-1003_1160-1002dup XP_024309019.1:n.1160-1003_1160-1002dup
XM_024453252.1:c.1160-1003_1160-1002dup XP_024309020.1:n.1160-1003_1160-1002dup
XM_024453253.1:c.1160-1003_1160-1002dup XP_024309021.1:n.1160-1003_1160-1002dup
XM_024453254.1:c.1160-1003_1160-1002dup XP_024309022.1:n.1160-1003_1160-1002dup
XM_024453255.1:c.1160-1003_1160-1002dup XP_024309023.1:n.1160-1003_1160-1002dup
XM_024453256.1:c.1160-1003_1160-1002dup XP_024309024.1:n.1160-1003_1160-1002dup
XR_001739081.2:n.2090-1003_2090-1002dup
XR_922686.3:n.2089-1003_2089-1002dup
NM_014668.4:c.1160-1003_1160-1002dup MANE Select NP_055483.2:n.1160-1003_1160-1002dup
NM_033090.3:c.1160-1003_1160-1002dup NP_149081.1:n.1160-1003_1160-1002dup
NM_148903.3:c.*291_*292dup NP_683701.2:n.*291_*292dup