Canonical Allele Identifier: CA2322412797

Gene: CDC37 MIR1181

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10403483G= , CM000681.2:g.10403483G=	GRCh38
NC_000019.9:g.10514159G= , CM000681.1:g.10514159G=	GRCh37
NC_000019.8:g.10375159G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_007065.4:c.-4C= (CDC37) MANE Select	NP_008996.1:n.-4C=
ENST00000222005.7:c.-4C= (CDC37) MANE Select	ENSP00000222005.1:n.-4C=
NM_007065.3:c.-4C= (CDC37)	NP_008996.1:n.-4C=
NR_031592.1:n.56C= (MIR1181)
ENST00000222005.6:c.-4C= (CDC37)	ENSP00000222005.1:n.-4C=
ENST00000588869.1:c.-4C= (CDC37)	ENSP00000464971.1:n.-4C=
ENST00000589629.5:c.-4C= (CDC37)	ENSP00000467747.1:n.-4C=
ENST00000591248.5:n.48C= (CDC37)
ENST00000593124.1:c.-4C= (CDC37)	ENSP00000465724.1:n.-4C=
XM_011527652.1:c.-4C= (CDC37)	XP_011525954.1:n.-4C=
XM_011527652.3:c.-4C= (CDC37)	XP_011525954.1:n.-4C=