Canonical Allele Identifier: CA2611442393

Gene: EBF3

Linked Data

• gnomAD v4: 10-129841105-AATCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129841108_129841111del , CM000672.2:g.129841108_129841111del	GRCh38
NC_000010.10:g.131639372_131639375del , CM000672.1:g.131639372_131639375del	GRCh37
NC_000010.9:g.131529362_131529365del	NCBI36
NG_030038.1:g.127719_127722del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355311.10:c.1373-77_1373-74del	ENSP00000347463.4:n.1373-77_1373-74del
ENST00000368648.8:c.1346-77_1346-74del	ENSP00000357637.3:n.1346-77_1346-74del
ENST00000440978.2:c.1373-77_1373-74del MANE Select	ENSP00000387543.2:n.1373-77_1373-74del
ENST00000675373.1:n.1018-77_1018-74del
ENST00000355311.9:c.1373-77_1373-74del	ENSP00000347463.4:n.1373-77_1373-74del
ENST00000368648.7:c.1346-77_1346-74del	ENSP00000357637.3:n.1346-77_1346-74del
ENST00000440978.1:c.57-77_57-74del
NM_001005463.2:c.1346-77_1346-74del	NP_001005463.1:n.1346-77_1346-74del
XM_005252667.2:c.1346-77_1346-74del	XP_005252724.1:n.1346-77_1346-74del
XM_005252668.2:c.1373-77_1373-74del	XP_005252725.1:n.1373-77_1373-74del
XM_005252669.2:c.1346-77_1346-74del	XP_005252726.1:n.1346-77_1346-74del
XM_006717739.2:c.1373-77_1373-74del	XP_006717802.1:n.1373-77_1373-74del
XM_006717740.2:c.1373-77_1373-74del	XP_006717803.1:n.1373-77_1373-74del
XM_006717741.2:c.1373-77_1373-74del	XP_006717804.1:n.1373-77_1373-74del
XM_006717742.2:c.1373-77_1373-74del	XP_006717805.1:n.1373-77_1373-74del
XM_006717743.2:c.1373-77_1373-74del	XP_006717806.1:n.1373-77_1373-74del
XM_006717744.2:c.1373-775_1373-772del	XP_006717807.1:n.1373-775_1373-772del
XM_011539574.1:c.1088-77_1088-74del	XP_011537876.1:n.1088-77_1088-74del
XM_011539575.1:c.857-77_857-74del	XP_011537877.1:n.857-77_857-74del
XM_005252667.3:c.1346-77_1346-74del	XP_005252724.1:n.1346-77_1346-74del
XM_005252668.3:c.1373-77_1373-74del	XP_005252725.1:n.1373-77_1373-74del
XM_005252669.3:c.1346-77_1346-74del	XP_005252726.1:n.1346-77_1346-74del
XM_006717739.3:c.1373-77_1373-74del	XP_006717802.1:n.1373-77_1373-74del
XM_006717740.3:c.1373-77_1373-74del	XP_006717803.1:n.1373-77_1373-74del
XM_006717741.3:c.1373-77_1373-74del	XP_006717804.1:n.1373-77_1373-74del
XM_006717742.3:c.1373-77_1373-74del	XP_006717805.1:n.1373-77_1373-74del
XM_006717743.3:c.1373-77_1373-74del	XP_006717806.1:n.1373-77_1373-74del
XM_006717744.3:c.1373-775_1373-772del	XP_006717807.1:n.1373-775_1373-772del
XM_011539574.2:c.1088-77_1088-74del	XP_011537876.1:n.1088-77_1088-74del
XM_011539575.2:c.857-77_857-74del	XP_011537877.1:n.857-77_857-74del
XM_017016027.1:c.1373-775_1373-772del	XP_016871516.1:n.1373-775_1373-772del
XR_001747076.1:n.1852-77_1852-74del
NM_001005463.3:c.1346-77_1346-74del	NP_001005463.1:n.1346-77_1346-74del
NM_001375379.1:c.1373-77_1373-74del	NP_001362308.1:n.1373-77_1373-74del
NM_001375380.1:c.1373-77_1373-74del MANE Select	NP_001362309.1:n.1373-77_1373-74del
NM_001375389.1:c.1373-77_1373-74del	NP_001362318.1:n.1373-77_1373-74del
NM_001375390.1:c.1346-77_1346-74del	NP_001362319.1:n.1346-77_1346-74del
NM_001375391.1:c.1373-77_1373-74del	NP_001362320.1:n.1373-77_1373-74del
NM_001375392.1:c.1346-667_1346-664del	NP_001362321.1:n.1346-667_1346-664del