Canonical Allele Identifier: CA4011609

Gene: MYB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135198956T>C , CM000668.2:g.135198956T>C	GRCh38
NC_000006.11:g.135520094T>C , CM000668.1:g.135520094T>C	GRCh37
NC_000006.10:g.135561787T>C	NCBI36
NG_012330.1:g.22642T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001130173.2:c.1615T>C MANE Select	NP_001123645.1:p.Ser539Pro
ENST00000341911.10:c.1615T>C MANE Select	ENSP00000339992.5:p.Ser539Pro
NM_001130172.1:c.1243T>C	NP_001123644.1:p.Ser415Pro
NM_001130172.2:c.1243T>C	NP_001123644.1:p.Ser415Pro
NM_001130173.1:c.1615T>C	NP_001123645.1:p.Ser539Pro
NM_001161656.1:c.1606T>C	NP_001155128.1:p.Ser536Pro
NM_001161656.2:c.1606T>C	NP_001155128.1:p.Ser536Pro
NM_001161657.1:c.997T>C	NP_001155129.1:p.Ser333Pro
NM_001161657.2:c.997T>C	NP_001155129.1:p.Ser333Pro
NM_001161658.1:c.1567T>C	NP_001155130.1:p.Ser523Pro
NM_001161658.2:c.1567T>C	NP_001155130.1:p.Ser523Pro
NM_001161659.1:c.1252T>C	NP_001155131.1:p.Ser418Pro
NM_001161659.2:c.1252T>C	NP_001155131.1:p.Ser418Pro
NM_001161660.1:c.1147T>C	NP_001155132.1:p.Ser383Pro
NM_001161660.2:c.1147T>C	NP_001155132.1:p.Ser383Pro
NM_005375.2:c.1252T>C	NP_005366.2:p.Ser418Pro
NM_005375.3:c.1252T>C	NP_005366.2:p.Ser418Pro
NM_005375.4:c.1252T>C	NP_005366.2:p.Ser418Pro
NR_134958.1:n.1573T>C
NR_134958.2:n.1580T>C
NR_134959.1:n.1564T>C
NR_134959.2:n.1571T>C
NR_134960.1:n.1451T>C
NR_134960.2:n.1458T>C
NR_134961.1:n.1634T>C
NR_134961.2:n.1641T>C
NR_134962.1:n.1352T>C
NR_134962.2:n.1359T>C
NR_134963.1:n.1451T>C
NR_134963.2:n.1458T>C
NR_134964.1:n.1442T>C
NR_134964.2:n.1449T>C
NR_134965.1:n.1573T>C
NR_134965.2:n.1580T>C
ENST00000316528.12:c.1252T>C	ENSP00000326328.8:p.Ser418Pro
ENST00000339290.9:c.1252T>C	ENSP00000341050.5:p.Ser418Pro
ENST00000341911.9:c.1615T>C	ENSP00000339992.5:p.Ser539Pro
ENST00000367812.6:c.1252T>C	ENSP00000356786.2:p.Ser418Pro
ENST00000367814.8:c.1252T>C	ENSP00000356788.4:p.Ser418Pro
ENST00000438901.6:c.1567T>C	ENSP00000413011.2:p.Ser523Pro
ENST00000442647.6:c.1243T>C	ENSP00000410825.2:p.Ser415Pro
ENST00000442647.7:c.1243T>C	ENSP00000410825.2:p.Ser415Pro
ENST00000463282.6:c.*321T>C	ENSP00000436602.1:n.*321T>C
ENST00000524588.5:c.959T>C	ENSP00000434675.1:n.959T>C
ENST00000525002.5:c.1252T>C	ENSP00000433745.1:p.Ser418Pro
ENST00000525369.5:c.997T>C	ENSP00000435938.1:p.Ser333Pro
ENST00000525477.5:c.*321T>C	ENSP00000437081.1:n.*321T>C
ENST00000525514.5:c.1374T>C	ENSP00000435578.1:n.1374T>C
ENST00000525940.5:c.1167T>C	ENSP00000432948.1:n.1167T>C
ENST00000526187.5:c.1521T>C	ENSP00000434795.1:n.1521T>C
ENST00000526320.5:c.1167T>C	ENSP00000434917.1:n.1167T>C
ENST00000526565.5:c.1728T>C	ENSP00000436385.1:n.1728T>C
ENST00000526889.5:c.1243T>C	ENSP00000433458.1:p.Ser415Pro
ENST00000527615.5:c.1252T>C	ENSP00000433227.1:p.Ser418Pro
ENST00000528015.5:c.1530T>C	ENSP00000434816.1:n.1530T>C
ENST00000528140.5:c.1350T>C	ENSP00000432877.1:n.1350T>C
ENST00000528343.5:c.1252T>C	ENSP00000434420.1:p.Ser418Pro
ENST00000528345.5:c.1302T>C	ENSP00000435497.1:n.1302T>C
ENST00000528774.5:c.1606T>C	ENSP00000434723.1:p.Ser536Pro
ENST00000529262.5:c.1756T>C	ENSP00000433844.1:n.1756T>C
ENST00000529586.5:c.1289T>C	ENSP00000437264.1:n.1289T>C
ENST00000531519.5:c.997T>C	ENSP00000435595.1:p.Ser333Pro
ENST00000531634.5:c.1153T>C	ENSP00000436925.1:n.1153T>C
ENST00000531737.5:c.1765T>C	ENSP00000432168.1:n.1765T>C
ENST00000531845.5:n.1368T>C
ENST00000533384.5:c.1850T>C	ENSP00000432811.1:n.1850T>C
ENST00000533624.5:c.1147T>C	ENSP00000436605.1:p.Ser383Pro
ENST00000533808.5:c.1435T>C	ENSP00000435293.1:n.1435T>C
ENST00000533837.5:c.*226T>C	ENSP00000434639.1:n.*226T>C
ENST00000534044.5:c.1252T>C	ENSP00000435055.1:p.Ser418Pro
ENST00000534121.5:c.1567T>C	ENSP00000432851.1:p.Ser523Pro
ENST00000616088.4:c.1252T>C	ENSP00000477898.1:p.Ser418Pro
ENST00000618728.4:c.1252T>C	ENSP00000479896.1:p.Ser418Pro
XR_001744367.1:n.368-2956A>G
XR_001744368.1:n.279-2956A>G
XR_942443.1:n.1785T>C
XR_942444.1:n.2148T>C
XR_942444.2:n.1773T>C
XR_942445.1:n.1776T>C
XR_942446.1:n.1907T>C
XR_943011.1:n.484-2956A>G
XR_943012.1:n.389-2956A>G
XR_943013.1:n.465-2956A>G
XR_943015.1:n.370-2956A>G