Canonical Allele Identifier: CA365735441

Gene: MYB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135192329A>G , CM000668.2:g.135192329A>G	GRCh38
NC_000006.11:g.135513467A>G , CM000668.1:g.135513467A>G	GRCh37
NC_000006.10:g.135555160A>G	NCBI36
NG_012330.1:g.16015A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341911.10:c.533A>G MANE Select	ENSP00000339992.5:p.Asp178Gly
ENST00000442647.7:c.533A>G	ENSP00000410825.2:p.Asp178Gly
ENST00000316528.12:c.533A>G	ENSP00000326328.8:p.Asp178Gly
ENST00000339290.9:c.533A>G	ENSP00000341050.5:p.Asp178Gly
ENST00000341911.9:c.533A>G	ENSP00000339992.5:p.Asp178Gly
ENST00000367812.6:c.533A>G	ENSP00000356786.2:p.Asp178Gly
ENST00000367814.8:c.533A>G	ENSP00000356788.4:p.Asp178Gly
ENST00000420123.6:c.461A>G	ENSP00000403387.2:p.Asp154Gly
ENST00000430686.2:c.395A>G	ENSP00000390460.2:p.Asp132Gly
ENST00000438901.6:c.533A>G	ENSP00000413011.2:p.Asp178Gly
ENST00000442647.6:c.533A>G	ENSP00000410825.2:p.Asp178Gly
ENST00000463282.6:c.533A>G	ENSP00000436602.1:p.Asp178Gly
ENST00000524588.5:c.240A>G	ENSP00000434675.1:p.Ter80Trp
ENST00000525002.5:c.533A>G	ENSP00000433745.1:p.Asp178Gly
ENST00000525369.5:c.533A>G	ENSP00000435938.1:p.Asp178Gly
ENST00000525477.5:c.533A>G	ENSP00000437081.1:p.Asp178Gly
ENST00000525514.5:c.533A>G	ENSP00000435578.1:p.Asp178Gly
ENST00000525940.5:c.533A>G	ENSP00000432948.1:p.Asp178Gly
ENST00000526187.5:c.533A>G	ENSP00000434795.1:p.Asp178Gly
ENST00000526320.5:c.533A>G	ENSP00000434917.1:p.Asp178Gly
ENST00000526565.5:c.533A>G	ENSP00000436385.1:p.Asp178Gly
ENST00000526889.5:c.533A>G	ENSP00000433458.1:p.Asp178Gly
ENST00000527615.5:c.533A>G	ENSP00000433227.1:p.Asp178Gly
ENST00000528015.5:c.533A>G	ENSP00000434816.1:p.Asp178Gly
ENST00000528140.5:c.533A>G	ENSP00000432877.1:p.Asp178Gly
ENST00000528343.5:c.533A>G	ENSP00000434420.1:p.Asp178Gly
ENST00000528345.5:c.461A>G	ENSP00000435497.1:p.Asp154Gly
ENST00000528774.5:c.533A>G	ENSP00000434723.1:p.Asp178Gly
ENST00000529262.5:c.533A>G	ENSP00000433844.1:p.Asp178Gly
ENST00000529586.5:c.533A>G	ENSP00000437264.1:p.Asp178Gly
ENST00000531519.5:c.533A>G	ENSP00000435595.1:p.Asp178Gly
ENST00000531634.5:c.312A>G	ENSP00000436925.1:p.Ter104Trp
ENST00000531737.5:c.533A>G	ENSP00000432168.1:p.Asp178Gly
ENST00000531845.5:n.536A>G
ENST00000533384.5:c.533A>G	ENSP00000432811.1:p.Asp178Gly
ENST00000533624.5:c.533A>G	ENSP00000436605.1:p.Asp178Gly
ENST00000533808.5:c.533A>G	ENSP00000435293.1:p.Asp178Gly
ENST00000533837.5:c.533A>G	ENSP00000434639.1:p.Asp178Gly
ENST00000534044.5:c.533A>G	ENSP00000435055.1:p.Asp178Gly
ENST00000534121.5:c.533A>G	ENSP00000432851.1:p.Asp178Gly
ENST00000616088.4:c.533A>G	ENSP00000477898.1:p.Asp178Gly
ENST00000618728.4:c.533A>G	ENSP00000479896.1:p.Asp178Gly
NM_001130172.1:c.533A>G	NP_001123644.1:p.Asp178Gly
NM_001130173.1:c.533A>G	NP_001123645.1:p.Asp178Gly
NM_001161656.1:c.533A>G	NP_001155128.1:p.Asp178Gly
NM_001161657.1:c.533A>G	NP_001155129.1:p.Asp178Gly
NM_001161658.1:c.533A>G	NP_001155130.1:p.Asp178Gly
NM_001161659.1:c.533A>G	NP_001155131.1:p.Asp178Gly
NM_001161660.1:c.533A>G	NP_001155132.1:p.Asp178Gly
NM_005375.2:c.533A>G	NP_005366.2:p.Asp178Gly
XR_942443.1:n.1066A>G
XR_942444.1:n.1066A>G
XR_942445.1:n.1066A>G
XR_942446.1:n.1066A>G
NM_005375.3:c.533A>G	NP_005366.2:p.Asp178Gly
NR_134958.1:n.732A>G
NR_134959.1:n.732A>G
NR_134960.1:n.732A>G
NR_134961.1:n.732A>G
NR_134962.1:n.511A>G
NR_134963.1:n.732A>G
NR_134964.1:n.732A>G
NR_134965.1:n.732A>G
XR_942444.2:n.691A>G
NM_001130173.2:c.533A>G MANE Select	NP_001123645.1:p.Asp178Gly
NM_001130172.2:c.533A>G	NP_001123644.1:p.Asp178Gly
NM_001161656.2:c.533A>G	NP_001155128.1:p.Asp178Gly
NM_001161657.2:c.533A>G	NP_001155129.1:p.Asp178Gly
NM_001161658.2:c.533A>G	NP_001155130.1:p.Asp178Gly
NM_001161659.2:c.533A>G	NP_001155131.1:p.Asp178Gly
NM_001161660.2:c.533A>G	NP_001155132.1:p.Asp178Gly
NM_005375.4:c.533A>G	NP_005366.2:p.Asp178Gly
NR_134958.2:n.739A>G
NR_134959.2:n.739A>G
NR_134960.2:n.739A>G
NR_134961.2:n.739A>G
NR_134962.2:n.518A>G
NR_134963.2:n.739A>G
NR_134964.2:n.739A>G
NR_134965.2:n.739A>G