Canonical Allele Identifier: CA365740993

Gene: MYB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135201717T>C , CM000668.2:g.135201717T>C	GRCh38
NC_000006.11:g.135522855T>C , CM000668.1:g.135522855T>C	GRCh37
NC_000006.10:g.135564548T>C	NCBI36
NG_012330.1:g.25403T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341911.10:c.2029T>C MANE Select	ENSP00000339992.5:p.Phe677Leu
ENST00000442647.7:c.1657T>C	ENSP00000410825.2:p.Phe553Leu
ENST00000316528.12:c.1666T>C	ENSP00000326328.8:p.Phe556Leu
ENST00000339290.9:c.*372T>C	ENSP00000341050.5:n.*372T>C
ENST00000341911.9:c.2029T>C	ENSP00000339992.5:p.Phe677Leu
ENST00000367812.6:c.1666T>C	ENSP00000356786.2:p.Phe556Leu
ENST00000367814.8:c.1666T>C	ENSP00000356788.4:p.Phe556Leu
ENST00000438901.6:c.2037T>C	ENSP00000413011.2:n.2037T>C
ENST00000442647.6:c.1657T>C	ENSP00000410825.2:p.Phe553Leu
ENST00000463282.6:c.*735T>C	ENSP00000436602.1:n.*735T>C
ENST00000524588.5:c.1373T>C	ENSP00000434675.1:n.1373T>C
ENST00000525002.5:c.1925T>C	ENSP00000433745.1:n.1925T>C
ENST00000525369.5:c.1411T>C	ENSP00000435938.1:p.Phe471Leu
ENST00000525477.5:c.*735T>C	ENSP00000437081.1:n.*735T>C
ENST00000525514.5:c.1844T>C	ENSP00000435578.1:n.1844T>C
ENST00000525940.5:c.1581T>C	ENSP00000432948.1:n.1581T>C
ENST00000526187.5:c.1935T>C	ENSP00000434795.1:n.1935T>C
ENST00000526320.5:c.1637T>C	ENSP00000434917.1:n.1637T>C
ENST00000526565.5:c.2142T>C	ENSP00000436385.1:n.2142T>C
ENST00000526889.5:c.1713T>C	ENSP00000433458.1:n.1713T>C
ENST00000527615.5:c.1666T>C	ENSP00000433227.1:p.Phe556Leu
ENST00000528015.5:c.1944T>C	ENSP00000434816.1:n.1944T>C
ENST00000528140.5:c.1764T>C	ENSP00000432877.1:n.1764T>C
ENST00000528343.5:c.1808T>C	ENSP00000434420.1:n.1808T>C
ENST00000528345.5:c.1716T>C	ENSP00000435497.1:n.1716T>C
ENST00000528774.5:c.2020T>C	ENSP00000434723.1:p.Phe674Leu
ENST00000529262.5:c.2170T>C	ENSP00000433844.1:n.2170T>C
ENST00000529586.5:c.1759T>C	ENSP00000437264.1:n.1759T>C
ENST00000531519.5:c.1467T>C	ENSP00000435595.1:n.1467T>C
ENST00000531634.5:c.1567T>C	ENSP00000436925.1:n.1567T>C
ENST00000531737.5:c.2179T>C	ENSP00000432168.1:n.2179T>C
ENST00000531845.5:n.1782T>C
ENST00000533384.5:c.2264T>C	ENSP00000432811.1:n.2264T>C
ENST00000533624.5:c.1561T>C	ENSP00000436605.1:p.Phe521Leu
ENST00000533808.5:c.1905T>C	ENSP00000435293.1:n.1905T>C
ENST00000533837.5:c.*640T>C	ENSP00000434639.1:n.*640T>C
ENST00000534044.5:c.1587+1302T>C	ENSP00000435055.1:n.1587+1302T>C
ENST00000534121.5:c.1981T>C	ENSP00000432851.1:p.Phe661Leu
ENST00000616088.4:c.1666T>C	ENSP00000477898.1:p.Phe556Leu
ENST00000618728.4:c.1666T>C	ENSP00000479896.1:p.Phe556Leu
NM_001130172.1:c.1657T>C	NP_001123644.1:p.Phe553Leu
NM_001130173.1:c.2029T>C	NP_001123645.1:p.Phe677Leu
NM_001161656.1:c.2020T>C	NP_001155128.1:p.Phe674Leu
NM_001161657.1:c.1411T>C	NP_001155129.1:p.Phe471Leu
NM_001161658.1:c.1981T>C	NP_001155130.1:p.Phe661Leu
NM_001161659.1:c.1587+1302T>C	NP_001155131.1:n.1587+1302T>C
NM_001161660.1:c.1561T>C	NP_001155132.1:p.Phe521Leu
NM_005375.2:c.1666T>C	NP_005366.2:p.Phe556Leu
XR_942443.1:n.2341T>C
XR_942445.1:n.2246T>C
XR_942446.1:n.2377T>C
XR_943011.1:n.484-5717A>G
XR_943012.1:n.389-5717A>G
XR_943013.1:n.465-5717A>G
XR_943015.1:n.370-5717A>G
NM_005375.3:c.1666T>C	NP_005366.2:p.Phe556Leu
NR_134958.1:n.1987T>C
NR_134959.1:n.1978T>C
NR_134960.1:n.1921T>C
NR_134961.1:n.2048T>C
NR_134962.1:n.1766T>C
NR_134963.1:n.2007T>C
NR_134964.1:n.1912T>C
NR_134965.1:n.2043T>C
XR_001744367.1:n.368-5717A>G
XR_001744368.1:n.279-5717A>G
NM_001130173.2:c.2029T>C MANE Select	NP_001123645.1:p.Phe677Leu
NM_001130172.2:c.1657T>C	NP_001123644.1:p.Phe553Leu
NM_001161656.2:c.2020T>C	NP_001155128.1:p.Phe674Leu
NM_001161657.2:c.1411T>C	NP_001155129.1:p.Phe471Leu
NM_001161658.2:c.1981T>C	NP_001155130.1:p.Phe661Leu
NM_001161659.2:c.1587+1302T>C	NP_001155131.1:n.1587+1302T>C
NM_001161660.2:c.1561T>C	NP_001155132.1:p.Phe521Leu
NM_005375.4:c.1666T>C	NP_005366.2:p.Phe556Leu
NR_134958.2:n.1994T>C
NR_134959.2:n.1985T>C
NR_134960.2:n.1928T>C
NR_134961.2:n.2055T>C
NR_134962.2:n.1773T>C
NR_134963.2:n.2014T>C
NR_134964.2:n.1919T>C
NR_134965.2:n.2050T>C