Canonical Allele Identifier: CA4767316

Gene: MYBL1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.66566141T>C , CM000670.2:g.66566141T>C	GRCh38
NC_000008.10:g.67478376T>C , CM000670.1:g.67478376T>C	GRCh37
NC_000008.9:g.67640930T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001080416.4:c.2053A>G MANE Select	NP_001073885.1:p.Asn685Asp
ENST00000522677.8:c.2053A>G MANE Select	ENSP00000429633.2:p.Asn685Asp
NM_001080416.3:c.2053A>G	NP_001073885.1:p.Asn685Asp
NM_001144755.2:c.1950+543A>G	NP_001138227.1:n.1950+543A>G
NM_001144755.3:c.1950+543A>G	NP_001138227.1:n.1950+543A>G
NM_001294282.1:c.1947+543A>G	NP_001281211.1:n.1947+543A>G
NM_001294282.2:c.1947+543A>G	NP_001281211.1:n.1947+543A>G
ENST00000517885.5:c.1027A>G	ENSP00000428265.1:p.Asn343Asp
ENST00000522419.1:n.188+543A>G
ENST00000522677.7:c.2053A>G	ENSP00000429633.2:p.Asn685Asp
ENST00000524176.2:c.1950+543A>G	ENSP00000428011.2:n.1950+543A>G
XM_011517533.1:c.2068A>G	XP_011515835.1:p.Asn690Asp
XM_011517533.3:c.2068A>G	XP_011515835.1:p.Asn690Asp
XM_011517534.1:c.2065A>G	XP_011515836.1:p.Asn689Asp
XM_011517535.1:c.1965+543A>G	XP_011515837.1:n.1965+543A>G
XM_011517535.3:c.1965+543A>G	XP_011515837.1:n.1965+543A>G
XM_017013455.1:c.2107A>G	XP_016868944.1:p.Asn703Asp
XM_017013456.1:c.2092A>G	XP_016868945.1:p.Asn698Asp
XM_017013457.1:c.2004+543A>G	XP_016868946.1:n.2004+543A>G
XM_017013458.1:c.1989+543A>G	XP_016868947.1:n.1989+543A>G