Canonical Allele Identifier: CA2748872148

Gene: GREB1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11587720_11587721insTC , CM000664.2:g.11587720_11587721insTC	GRCh38
NC_000002.11:g.11727846_11727847insTC , CM000664.1:g.11727846_11727847insTC	GRCh37
NC_000002.10:g.11645297_11645298insTC	NCBI36
NG_029429.1:g.58605_58606insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381486.7:c.1160-1026_1160-1025insTC MANE Select	ENSP00000370896.2:n.1160-1026_1160-1025insTC
ENST00000234142.9:c.1160-1026_1160-1025insTC	ENSP00000234142.5:n.1160-1026_1160-1025insTC
ENST00000263834.9:c.*268_*269insTC	ENSP00000263834.5:n.*268_*269insTC
ENST00000381483.6:c.1160-1026_1160-1025insTC	ENSP00000370892.2:n.1160-1026_1160-1025insTC
ENST00000381486.6:c.1160-1026_1160-1025insTC	ENSP00000370896.2:n.1160-1026_1160-1025insTC
NM_014668.3:c.1160-1026_1160-1025insTC	NP_055483.2:n.1160-1026_1160-1025insTC
NM_033090.2:c.1160-1026_1160-1025insTC	NP_149081.1:n.1160-1026_1160-1025insTC
NM_148903.2:c.*268_*269insTC	NP_683701.2:n.*268_*269insTC
XM_005246192.3:c.1160-1026_1160-1025insTC	XP_005246249.1:n.1160-1026_1160-1025insTC
XM_011510418.1:c.1160-1026_1160-1025insTC	XP_011508720.1:n.1160-1026_1160-1025insTC
XM_011510419.1:c.1160-1026_1160-1025insTC	XP_011508721.1:n.1160-1026_1160-1025insTC
XM_011510420.1:c.1160-1026_1160-1025insTC	XP_011508722.1:n.1160-1026_1160-1025insTC
XM_011510421.1:c.1160-1026_1160-1025insTC	XP_011508723.1:n.1160-1026_1160-1025insTC
XM_011510423.1:c.1160-1026_1160-1025insTC	XP_011508725.1:n.1160-1026_1160-1025insTC
XR_922686.1:n.1321-1026_1321-1025insTC
XM_005246192.4:c.1160-1026_1160-1025insTC	XP_005246249.1:n.1160-1026_1160-1025insTC
XM_011510418.3:c.1160-1026_1160-1025insTC	XP_011508720.1:n.1160-1026_1160-1025insTC
XM_011510419.3:c.1160-1026_1160-1025insTC	XP_011508721.1:n.1160-1026_1160-1025insTC
XM_011510423.3:c.1160-1026_1160-1025insTC	XP_011508725.1:n.1160-1026_1160-1025insTC
XM_024453250.1:c.1160-1026_1160-1025insTC	XP_024309018.1:n.1160-1026_1160-1025insTC
XM_024453251.1:c.1160-1026_1160-1025insTC	XP_024309019.1:n.1160-1026_1160-1025insTC
XM_024453252.1:c.1160-1026_1160-1025insTC	XP_024309020.1:n.1160-1026_1160-1025insTC
XM_024453253.1:c.1160-1026_1160-1025insTC	XP_024309021.1:n.1160-1026_1160-1025insTC
XM_024453254.1:c.1160-1026_1160-1025insTC	XP_024309022.1:n.1160-1026_1160-1025insTC
XM_024453255.1:c.1160-1026_1160-1025insTC	XP_024309023.1:n.1160-1026_1160-1025insTC
XM_024453256.1:c.1160-1026_1160-1025insTC	XP_024309024.1:n.1160-1026_1160-1025insTC
XR_001739081.2:n.2090-1026_2090-1025insTC
XR_922686.3:n.2089-1026_2089-1025insTC
NM_014668.4:c.1160-1026_1160-1025insTC MANE Select	NP_055483.2:n.1160-1026_1160-1025insTC
NM_033090.3:c.1160-1026_1160-1025insTC	NP_149081.1:n.1160-1026_1160-1025insTC
NM_148903.3:c.*268_*269insTC	NP_683701.2:n.*268_*269insTC