Canonical Allele Identifier: CA4011642

Gene: MYB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135200101A>G , CM000668.2:g.135200101A>G	GRCh38
NC_000006.11:g.135521239A>G , CM000668.1:g.135521239A>G	GRCh37
NC_000006.10:g.135562932A>G	NCBI36
NG_012330.1:g.23787A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341911.10:c.1726A>G MANE Select	ENSP00000339992.5:p.Ile576Val
ENST00000442647.7:c.1354A>G	ENSP00000410825.2:p.Ile452Val
ENST00000316528.12:c.1363A>G	ENSP00000326328.8:p.Ile455Val
ENST00000339290.9:c.*69A>G	ENSP00000341050.5:n.*69A>G
ENST00000341911.9:c.1726A>G	ENSP00000339992.5:p.Ile576Val
ENST00000367812.6:c.1363A>G	ENSP00000356786.2:p.Ile455Val
ENST00000367814.8:c.1363A>G	ENSP00000356788.4:p.Ile455Val
ENST00000438901.6:c.1734A>G	ENSP00000413011.2:n.1734A>G
ENST00000442647.6:c.1354A>G	ENSP00000410825.2:p.Ile452Val
ENST00000463282.6:c.*432A>G	ENSP00000436602.1:n.*432A>G
ENST00000524588.5:c.1070A>G	ENSP00000434675.1:n.1070A>G
ENST00000525002.5:c.1363A>G	ENSP00000433745.1:p.Ile455Val
ENST00000525369.5:c.1108A>G	ENSP00000435938.1:p.Ile370Val
ENST00000525477.5:c.*432A>G	ENSP00000437081.1:n.*432A>G
ENST00000525514.5:c.1541A>G	ENSP00000435578.1:n.1541A>G
ENST00000525940.5:c.1278A>G	ENSP00000432948.1:n.1278A>G
ENST00000526187.5:c.1632A>G	ENSP00000434795.1:n.1632A>G
ENST00000526320.5:c.1334A>G	ENSP00000434917.1:n.1334A>G
ENST00000526565.5:c.1839A>G	ENSP00000436385.1:n.1839A>G
ENST00000526889.5:c.1410A>G	ENSP00000433458.1:n.1410A>G
ENST00000527615.5:c.1363A>G	ENSP00000433227.1:p.Ile455Val
ENST00000528015.5:c.1641A>G	ENSP00000434816.1:n.1641A>G
ENST00000528140.5:c.1461A>G	ENSP00000432877.1:n.1461A>G
ENST00000528343.5:c.1363A>G	ENSP00000434420.1:p.Ile455Val
ENST00000528345.5:c.1413A>G	ENSP00000435497.1:n.1413A>G
ENST00000528774.5:c.1717A>G	ENSP00000434723.1:p.Ile573Val
ENST00000529262.5:c.1867A>G	ENSP00000433844.1:n.1867A>G
ENST00000529586.5:c.1456A>G	ENSP00000437264.1:n.1456A>G
ENST00000531519.5:c.1164A>G	ENSP00000435595.1:n.1164A>G
ENST00000531634.5:c.1264A>G	ENSP00000436925.1:n.1264A>G
ENST00000531737.5:c.1876A>G	ENSP00000432168.1:n.1876A>G
ENST00000531845.5:n.1479A>G
ENST00000533384.5:c.1961A>G	ENSP00000432811.1:n.1961A>G
ENST00000533624.5:c.1258A>G	ENSP00000436605.1:p.Ile420Val
ENST00000533808.5:c.1602A>G	ENSP00000435293.1:n.1602A>G
ENST00000533837.5:c.*337A>G	ENSP00000434639.1:n.*337A>G
ENST00000534044.5:c.1363A>G	ENSP00000435055.1:p.Ile455Val
ENST00000534121.5:c.1678A>G	ENSP00000432851.1:p.Ile560Val
ENST00000616088.4:c.1363A>G	ENSP00000477898.1:p.Ile455Val
ENST00000618728.4:c.1363A>G	ENSP00000479896.1:p.Ile455Val
NM_001130172.1:c.1354A>G	NP_001123644.1:p.Ile452Val
NM_001130173.1:c.1726A>G	NP_001123645.1:p.Ile576Val
NM_001161656.1:c.1717A>G	NP_001155128.1:p.Ile573Val
NM_001161657.1:c.1108A>G	NP_001155129.1:p.Ile370Val
NM_001161658.1:c.1678A>G	NP_001155130.1:p.Ile560Val
NM_001161659.1:c.1363A>G	NP_001155131.1:p.Ile455Val
NM_001161660.1:c.1258A>G	NP_001155132.1:p.Ile420Val
NM_005375.2:c.1363A>G	NP_005366.2:p.Ile455Val
XR_942443.1:n.1896A>G
XR_942444.1:n.2315A>G
XR_942445.1:n.1943A>G
XR_942446.1:n.2074A>G
XR_943011.1:n.484-4101T>C
XR_943012.1:n.389-4101T>C
XR_943013.1:n.465-4101T>C
XR_943015.1:n.370-4101T>C
NM_005375.3:c.1363A>G	NP_005366.2:p.Ile455Val
NR_134958.1:n.1684A>G
NR_134959.1:n.1675A>G
NR_134960.1:n.1618A>G
NR_134961.1:n.1745A>G
NR_134962.1:n.1463A>G
NR_134963.1:n.1562A>G
NR_134964.1:n.1609A>G
NR_134965.1:n.1740A>G
XR_001744367.1:n.368-4101T>C
XR_001744368.1:n.279-4101T>C
XR_942444.2:n.1940A>G
NM_001130173.2:c.1726A>G MANE Select	NP_001123645.1:p.Ile576Val
NM_001130172.2:c.1354A>G	NP_001123644.1:p.Ile452Val
NM_001161656.2:c.1717A>G	NP_001155128.1:p.Ile573Val
NM_001161657.2:c.1108A>G	NP_001155129.1:p.Ile370Val
NM_001161658.2:c.1678A>G	NP_001155130.1:p.Ile560Val
NM_001161659.2:c.1363A>G	NP_001155131.1:p.Ile455Val
NM_001161660.2:c.1258A>G	NP_001155132.1:p.Ile420Val
NM_005375.4:c.1363A>G	NP_005366.2:p.Ile455Val
NR_134958.2:n.1691A>G
NR_134959.2:n.1682A>G
NR_134960.2:n.1625A>G
NR_134961.2:n.1752A>G
NR_134962.2:n.1470A>G
NR_134963.2:n.1569A>G
NR_134964.2:n.1616A>G
NR_134965.2:n.1747A>G