Canonical Allele Identifier: CA2614831855

Gene: CTTN

Linked Data

• gnomAD v4: 11-70434888-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70434888G>C , CM000673.2:g.70434888G>C	GRCh38
NC_000011.9:g.70280994G>C , CM000673.1:g.70280994G>C	GRCh37
NC_000011.8:g.69958642G>C	NCBI36
NG_029881.1:g.41383G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000301843.13:c.1517-138G>C MANE Select	ENSP00000301843.8:n.1517-138G>C
ENST00000301843.12:c.1517-138G>C	ENSP00000301843.8:n.1517-138G>C
ENST00000346329.7:c.1406-138G>C	ENSP00000317189.4:n.1406-138G>C
ENST00000376561.7:c.1406-138G>C	ENSP00000365745.3:n.1406-138G>C
ENST00000393747.3:n.706-138G>C
ENST00000529736.5:c.488-138G>C	ENSP00000431421.1:n.488-138G>C
ENST00000533931.1:c.441-138G>C	ENSP00000436613.1:n.441-138G>C
NM_001184740.1:c.1406-138G>C	NP_001171669.1:n.1406-138G>C
NM_005231.3:c.1517-138G>C	NP_005222.2:n.1517-138G>C
NM_138565.2:c.1406-138G>C	NP_612632.1:n.1406-138G>C
XM_006718447.2:c.1295-138G>C	XP_006718510.1:n.1295-138G>C
XM_006718447.3:c.1295-138G>C	XP_006718510.1:n.1295-138G>C
NM_005231.4:c.1517-138G>C MANE Select	NP_005222.2:n.1517-138G>C
NM_001184740.2:c.1406-138G>C	NP_001171669.1:n.1406-138G>C
NM_138565.3:c.1406-138G>C	NP_612632.1:n.1406-138G>C