Canonical Allele Identifier: CA1981049207

Gene: CTTN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70434896G= , CM000673.2:g.70434896G=	GRCh38
NC_000011.9:g.70281002G= , CM000673.1:g.70281002G=	GRCh37
NC_000011.8:g.69958650G=	NCBI36
NG_029881.1:g.41391G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000301843.13:c.1517-130G= MANE Select	ENSP00000301843.8:n.1517-130G=
ENST00000301843.12:c.1517-130G=	ENSP00000301843.8:n.1517-130G=
ENST00000346329.7:c.1406-130G=	ENSP00000317189.4:n.1406-130G=
ENST00000376561.7:c.1406-130G=	ENSP00000365745.3:n.1406-130G=
ENST00000393747.3:n.706-130G=
ENST00000529736.5:c.488-130G=	ENSP00000431421.1:n.488-130G=
ENST00000533931.1:c.441-130G=	ENSP00000436613.1:n.441-130G=
NM_001184740.1:c.1406-130G=	NP_001171669.1:n.1406-130G=
NM_005231.3:c.1517-130G=	NP_005222.2:n.1517-130G=
NM_138565.2:c.1406-130G=	NP_612632.1:n.1406-130G=
XM_006718447.2:c.1295-130G=	XP_006718510.1:n.1295-130G=
XM_006718447.3:c.1295-130G=	XP_006718510.1:n.1295-130G=
NM_005231.4:c.1517-130G= MANE Select	NP_005222.2:n.1517-130G=
NM_001184740.2:c.1406-130G=	NP_001171669.1:n.1406-130G=
NM_138565.3:c.1406-130G=	NP_612632.1:n.1406-130G=