Canonical Allele Identifier: CA4767440

Gene: MYBL1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.66576041G>A , CM000670.2:g.66576041G>A	GRCh38
NC_000008.10:g.67488276G>A , CM000670.1:g.67488276G>A	GRCh37
NC_000008.9:g.67650830G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001080416.4:c.1436C>T MANE Select	NP_001073885.1:p.Thr479Ile
ENST00000522677.8:c.1436C>T MANE Select	ENSP00000429633.2:p.Thr479Ile
NM_001080416.3:c.1436C>T	NP_001073885.1:p.Thr479Ile
NM_001144755.2:c.1436C>T	NP_001138227.1:p.Thr479Ile
NM_001144755.3:c.1436C>T	NP_001138227.1:p.Thr479Ile
NM_001294282.1:c.1433C>T	NP_001281211.1:p.Thr478Ile
NM_001294282.2:c.1433C>T	NP_001281211.1:p.Thr478Ile
ENST00000517885.5:c.410C>T	ENSP00000428265.1:p.Thr137Ile
ENST00000522677.7:c.1436C>T	ENSP00000429633.2:p.Thr479Ile
ENST00000524176.2:c.1436C>T	ENSP00000428011.2:p.Thr479Ile
XM_011517533.1:c.1451C>T	XP_011515835.1:p.Thr484Ile
XM_011517533.3:c.1451C>T	XP_011515835.1:p.Thr484Ile
XM_011517534.1:c.1448C>T	XP_011515836.1:p.Thr483Ile
XM_011517535.1:c.1451C>T	XP_011515837.1:p.Thr484Ile
XM_011517535.3:c.1451C>T	XP_011515837.1:p.Thr484Ile
XM_011517536.1:c.1451C>T	XP_011515838.1:p.Thr484Ile
XM_017013455.1:c.1490C>T	XP_016868944.1:p.Thr497Ile
XM_017013456.1:c.1475C>T	XP_016868945.1:p.Thr492Ile
XM_017013457.1:c.1490C>T	XP_016868946.1:p.Thr497Ile
XM_017013458.1:c.1475C>T	XP_016868947.1:p.Thr492Ile
XM_017013459.1:c.1490C>T	XP_016868948.1:p.Thr497Ile