Canonical Allele Identifier: CA9194062

Gene: CDC37

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10393282C>T , CM000681.2:g.10393282C>T	GRCh38
NC_000019.9:g.10503958C>T , CM000681.1:g.10503958C>T	GRCh37
NC_000019.8:g.10364958C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222005.7:c.886G>A MANE Select	ENSP00000222005.1:p.Glu296Lys
ENST00000222005.6:c.886G>A	ENSP00000222005.1:p.Glu296Lys
ENST00000589331.1:c.132G>A
ENST00000589625.5:c.324G>A
ENST00000589629.5:c.604G>A	ENSP00000467747.1:p.Glu202Lys
ENST00000590632.1:n.505G>A
ENST00000591248.5:n.1028G>A
ENST00000593124.1:c.1039G>A	ENSP00000465724.1:p.Glu347Lys
NM_007065.3:c.886G>A	NP_008996.1:p.Glu296Lys
XM_011527652.1:c.1039G>A	XP_011525954.1:p.Glu347Lys
XM_011527652.3:c.1039G>A	XP_011525954.1:p.Glu347Lys
NM_007065.4:c.886G>A MANE Select	NP_008996.1:p.Glu296Lys