Canonical Allele Identifier: CA1981049213

Gene: CTTN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70434900_70434901delinsGT , CM000673.2:g.70434900_70434901delinsGT	GRCh38
NC_000011.9:g.70281006_70281007delinsGT , CM000673.1:g.70281006_70281007delinsGT	GRCh37
NC_000011.8:g.69958654_69958655delinsGT	NCBI36
NG_029881.1:g.41395_41396delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000301843.13:c.1517-126_1517-125delinsGT MANE Select	ENSP00000301843.8:n.1517-126_1517-125deli...
ENST00000301843.12:c.1517-126_1517-125delinsGT	ENSP00000301843.8:n.1517-126_1517-125deli...
ENST00000346329.7:c.1406-126_1406-125delinsGT	ENSP00000317189.4:n.1406-126_1406-125deli...
ENST00000376561.7:c.1406-126_1406-125delinsGT	ENSP00000365745.3:n.1406-126_1406-125deli...
ENST00000393747.3:n.706-126_706-125delinsGT
ENST00000529736.5:c.488-126_488-125delinsGT	ENSP00000431421.1:n.488-126_488-125delins...
ENST00000533931.1:c.441-126_441-125delinsGT	ENSP00000436613.1:n.441-126_441-125delins...
NM_001184740.1:c.1406-126_1406-125delinsGT	NP_001171669.1:n.1406-126_1406-125delinsG...
NM_005231.3:c.1517-126_1517-125delinsGT	NP_005222.2:n.1517-126_1517-125delinsGT
NM_138565.2:c.1406-126_1406-125delinsGT	NP_612632.1:n.1406-126_1406-125delinsGT
XM_006718447.2:c.1295-126_1295-125delinsGT	XP_006718510.1:n.1295-126_1295-125delinsG...
XM_006718447.3:c.1295-126_1295-125delinsGT	XP_006718510.1:n.1295-126_1295-125delinsG...
NM_005231.4:c.1517-126_1517-125delinsGT MANE Select	NP_005222.2:n.1517-126_1517-125delinsGT
NM_001184740.2:c.1406-126_1406-125delinsGT	NP_001171669.1:n.1406-126_1406-125delinsG...
NM_138565.3:c.1406-126_1406-125delinsGT	NP_612632.1:n.1406-126_1406-125delinsGT