Canonical Allele Identifier: CA4011861

Gene: MYB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135217921T>C , CM000668.2:g.135217921T>C	GRCh38
NC_000006.11:g.135539059T>C , CM000668.1:g.135539059T>C	GRCh37
NC_000006.10:g.135580752T>C	NCBI36
NG_012330.1:g.41607T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341911.10:c.2227T>C MANE Select	ENSP00000339992.5:p.Ser743Pro
ENST00000442647.7:c.1855T>C	ENSP00000410825.2:p.Ser619Pro
ENST00000316528.12:c.2122T>C	ENSP00000326328.8:p.Ser708Pro
ENST00000339290.9:c.*570T>C	ENSP00000341050.5:n.*570T>C
ENST00000341911.9:c.2227T>C	ENSP00000339992.5:p.Ser743Pro
ENST00000367812.6:c.*119T>C	ENSP00000356786.2:n.*119T>C
ENST00000367814.8:c.1864T>C	ENSP00000356788.4:p.Ser622Pro
ENST00000438901.6:c.2235T>C	ENSP00000413011.2:n.2235T>C
ENST00000442647.6:c.1855T>C	ENSP00000410825.2:p.Ser619Pro
ENST00000463282.6:c.*933T>C	ENSP00000436602.1:n.*933T>C
ENST00000524588.5:c.1571T>C	ENSP00000434675.1:n.1571T>C
ENST00000525002.5:c.2123T>C	ENSP00000433745.1:n.2123T>C
ENST00000525369.5:c.1609T>C	ENSP00000435938.1:p.Ser537Pro
ENST00000525477.5:c.*933T>C	ENSP00000437081.1:n.*933T>C
ENST00000525514.5:c.2042T>C	ENSP00000435578.1:n.2042T>C
ENST00000525940.5:c.1779T>C	ENSP00000432948.1:n.1779T>C
ENST00000526187.5:c.2133T>C	ENSP00000434795.1:n.2133T>C
ENST00000526320.5:c.1835T>C	ENSP00000434917.1:n.1835T>C
ENST00000526565.5:c.2340T>C	ENSP00000436385.1:n.2340T>C
ENST00000526889.5:c.1911T>C	ENSP00000433458.1:n.1911T>C
ENST00000528015.5:c.2142T>C	ENSP00000434816.1:n.2142T>C
ENST00000528140.5:c.1962T>C	ENSP00000432877.1:n.1962T>C
ENST00000528343.5:c.2006T>C	ENSP00000434420.1:n.2006T>C
ENST00000528345.5:c.1914T>C	ENSP00000435497.1:n.1914T>C
ENST00000528774.5:c.2218T>C	ENSP00000434723.1:p.Ser740Pro
ENST00000529262.5:c.2368T>C	ENSP00000433844.1:n.2368T>C
ENST00000529586.5:c.1957T>C	ENSP00000437264.1:n.1957T>C
ENST00000531519.5:c.1665T>C	ENSP00000435595.1:n.1665T>C
ENST00000531634.5:c.1765T>C	ENSP00000436925.1:n.1765T>C
ENST00000531737.5:c.2377T>C	ENSP00000432168.1:n.2377T>C
ENST00000531845.5:n.1980T>C
ENST00000533384.5:c.2462T>C	ENSP00000432811.1:n.2462T>C
ENST00000533624.5:c.1759T>C	ENSP00000436605.1:p.Ser587Pro
ENST00000533808.5:c.2103T>C	ENSP00000435293.1:n.2103T>C
ENST00000533837.5:c.*838T>C	ENSP00000434639.1:n.*838T>C
ENST00000534044.5:c.1753T>C	ENSP00000435055.1:p.Ser585Pro
ENST00000534121.5:c.2179T>C	ENSP00000432851.1:p.Ser727Pro
ENST00000616088.4:c.*141T>C	ENSP00000477898.1:n.*141T>C
ENST00000618728.4:c.*261T>C	ENSP00000479896.1:n.*261T>C
NM_001130172.1:c.1855T>C	NP_001123644.1:p.Ser619Pro
NM_001130173.1:c.2227T>C	NP_001123645.1:p.Ser743Pro
NM_001161656.1:c.2218T>C	NP_001155128.1:p.Ser740Pro
NM_001161657.1:c.1609T>C	NP_001155129.1:p.Ser537Pro
NM_001161658.1:c.2179T>C	NP_001155130.1:p.Ser727Pro
NM_001161659.1:c.1753T>C	NP_001155131.1:p.Ser585Pro
NM_001161660.1:c.1759T>C	NP_001155132.1:p.Ser587Pro
NM_005375.2:c.1864T>C	NP_005366.2:p.Ser622Pro
XR_942443.1:n.2539T>C
XR_942445.1:n.2444T>C
XR_942446.1:n.2575T>C
XR_943011.1:n.172-29A>G
XR_943012.1:n.172-29A>G
XR_943013.1:n.153-29A>G
XR_943015.1:n.153-29A>G
NM_005375.3:c.1864T>C	NP_005366.2:p.Ser622Pro
NR_134958.1:n.2185T>C
NR_134959.1:n.2176T>C
NR_134960.1:n.2119T>C
NR_134961.1:n.2246T>C
NR_134962.1:n.1964T>C
NR_134963.1:n.2205T>C
NR_134964.1:n.2110T>C
NR_134965.1:n.2241T>C
XR_001744368.1:n.177-2421A>G
NM_001130173.2:c.2227T>C MANE Select	NP_001123645.1:p.Ser743Pro
NM_001130172.2:c.1855T>C	NP_001123644.1:p.Ser619Pro
NM_001161656.2:c.2218T>C	NP_001155128.1:p.Ser740Pro
NM_001161657.2:c.1609T>C	NP_001155129.1:p.Ser537Pro
NM_001161658.2:c.2179T>C	NP_001155130.1:p.Ser727Pro
NM_001161659.2:c.1753T>C	NP_001155131.1:p.Ser585Pro
NM_001161660.2:c.1759T>C	NP_001155132.1:p.Ser587Pro
NM_005375.4:c.1864T>C	NP_005366.2:p.Ser622Pro
NR_134958.2:n.2192T>C
NR_134959.2:n.2183T>C
NR_134960.2:n.2126T>C
NR_134961.2:n.2253T>C
NR_134962.2:n.1971T>C
NR_134963.2:n.2212T>C
NR_134964.2:n.2117T>C
NR_134965.2:n.2248T>C