Canonical Allele Identifier: CA1531524785

Gene: CDH18

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.20374104C= , CM000667.2:g.20374104C=	GRCh38
NC_000005.9:g.20374213C= , CM000667.1:g.20374213C=	GRCh37
NC_000005.8:g.20409970C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001291956.1:c.-579-118599G=	NP_001278885.1:n.-579-118599G=
NM_001291956.2:c.-579-118599G=	NP_001278885.1:n.-579-118599G=
NM_001291956.3:c.-579-118599G=	NP_001278885.1:n.-579-118599G=
NM_001349556.1:c.-433-118599G=	NP_001336485.1:n.-433-118599G=
NM_001349556.2:c.-433-118599G=	NP_001336485.1:n.-433-118599G=
NM_001349558.1:c.-727-35865G=	NP_001336487.1:n.-727-35865G=
NM_001349558.2:c.-727-35865G=	NP_001336487.1:n.-727-35865G=
NM_001349562.1:c.-1076-118599G=	NP_001336491.1:n.-1076-118599G=
NM_001349562.2:c.-1076-118599G=	NP_001336491.1:n.-1076-118599G=
ENST00000507632.2:n.403-118599G=
ENST00000507958.5:c.-579-118599G=	ENSP00000425093.1:n.-579-118599G=
XM_005248228.2:c.-318-118599G=	XP_005248285.1:n.-318-118599G=
XM_005248228.4:c.-318-118599G=	XP_005248285.1:n.-318-118599G=
XM_017008924.2:c.-437-118599G=	XP_016864413.1:n.-437-118599G=
XM_017008926.2:c.-438+114243G=	XP_016864415.1:n.-438+114243G=
XM_017008928.2:c.-438+114243G=	XP_016864417.1:n.-438+114243G=