Canonical Allele Identifier: CA2489059090

Gene: GREB1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11587315_11587316delinsCT , CM000664.2:g.11587315_11587316delinsCT	GRCh38
NC_000002.11:g.11727441_11727442delinsCT , CM000664.1:g.11727441_11727442delinsCT	GRCh37
NC_000002.10:g.11644892_11644893delinsCT	NCBI36
NG_029429.1:g.58200_58201delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381486.7:c.1159+1410_1159+1411delinsCT MANE Select	ENSP00000370896.2:n.1159+1410_1159+1411delinsCT
ENST00000234142.9:c.1159+1410_1159+1411delinsCT	ENSP00000234142.5:n.1159+1410_1159+1411delinsCT
ENST00000263834.9:c.1160-67_1160-66delinsCT	ENSP00000263834.5:n.1160-67_1160-66delinsCT
ENST00000381483.6:c.1159+1410_1159+1411delinsCT	ENSP00000370892.2:n.1159+1410_1159+1411delinsCT
ENST00000381486.6:c.1159+1410_1159+1411delinsCT	ENSP00000370896.2:n.1159+1410_1159+1411delinsCT
NM_014668.3:c.1159+1410_1159+1411delinsCT	NP_055483.2:n.1159+1410_1159+1411delinsCT
NM_033090.2:c.1159+1410_1159+1411delinsCT	NP_149081.1:n.1159+1410_1159+1411delinsCT
NM_148903.2:c.1160-67_1160-66delinsCT	NP_683701.2:n.1160-67_1160-66delinsCT
XM_005246192.3:c.1159+1410_1159+1411delinsCT	XP_005246249.1:n.1159+1410_1159+1411delinsCT
XM_011510418.1:c.1159+1410_1159+1411delinsCT	XP_011508720.1:n.1159+1410_1159+1411delinsCT
XM_011510419.1:c.1159+1410_1159+1411delinsCT	XP_011508721.1:n.1159+1410_1159+1411delinsCT
XM_011510420.1:c.1159+1410_1159+1411delinsCT	XP_011508722.1:n.1159+1410_1159+1411delinsCT
XM_011510421.1:c.1159+1410_1159+1411delinsCT	XP_011508723.1:n.1159+1410_1159+1411delinsCT
XM_011510423.1:c.1159+1410_1159+1411delinsCT	XP_011508725.1:n.1159+1410_1159+1411delinsCT
XR_922686.1:n.1320+1410_1320+1411delinsCT
XM_005246192.4:c.1159+1410_1159+1411delinsCT	XP_005246249.1:n.1159+1410_1159+1411delinsCT
XM_011510418.3:c.1159+1410_1159+1411delinsCT	XP_011508720.1:n.1159+1410_1159+1411delinsCT
XM_011510419.3:c.1159+1410_1159+1411delinsCT	XP_011508721.1:n.1159+1410_1159+1411delinsCT
XM_011510423.3:c.1159+1410_1159+1411delinsCT	XP_011508725.1:n.1159+1410_1159+1411delinsCT
XM_024453250.1:c.1159+1410_1159+1411delinsCT	XP_024309018.1:n.1159+1410_1159+1411delinsCT
XM_024453251.1:c.1159+1410_1159+1411delinsCT	XP_024309019.1:n.1159+1410_1159+1411delinsCT
XM_024453252.1:c.1159+1410_1159+1411delinsCT	XP_024309020.1:n.1159+1410_1159+1411delinsCT
XM_024453253.1:c.1159+1410_1159+1411delinsCT	XP_024309021.1:n.1159+1410_1159+1411delinsCT
XM_024453254.1:c.1159+1410_1159+1411delinsCT	XP_024309022.1:n.1159+1410_1159+1411delinsCT
XM_024453255.1:c.1159+1410_1159+1411delinsCT	XP_024309023.1:n.1159+1410_1159+1411delinsCT
XM_024453256.1:c.1159+1410_1159+1411delinsCT	XP_024309024.1:n.1159+1410_1159+1411delinsCT
XR_001739081.2:n.2089+1410_2089+1411delinsCT
XR_922686.3:n.2088+1410_2088+1411delinsCT
NM_014668.4:c.1159+1410_1159+1411delinsCT MANE Select	NP_055483.2:n.1159+1410_1159+1411delinsCT
NM_033090.3:c.1159+1410_1159+1411delinsCT	NP_149081.1:n.1159+1410_1159+1411delinsCT
NM_148903.3:c.1160-67_1160-66delinsCT	NP_683701.2:n.1160-67_1160-66delinsCT