Canonical Allele Identifier: CA444855352

Gene: OCLN

Linked Data

• MyVariant Identifiers: chr5:g.68830643A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.69534816A>C , CM000667.2:g.69534816A>C	GRCh38
NC_000005.9:g.68830643A>C , CM000667.1:g.68830643A>C	GRCh37
NC_000005.8:g.68866399A>C	NCBI36
NG_028291.1:g.47525A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396442.7:c.1014A>C MANE Select	ENSP00000379719.2:p.Pro338=
ENST00000680027.1:c.1014A>C	ENSP00000506162.1:p.Pro338=
ENST00000680496.1:c.852A>C	ENSP00000504966.1:p.Pro284=
ENST00000680784.1:c.852A>C	ENSP00000506305.1:p.Pro284=
ENST00000681041.1:c.1014A>C	ENSP00000505426.1:p.Pro338=
ENST00000681586.1:c.1014A>C	ENSP00000505541.1:p.Pro338=
ENST00000681588.1:c.*190A>C	ENSP00000506017.1:n.*190A>C
ENST00000681895.1:c.1014A>C	ENSP00000505831.1:p.Pro338=
ENST00000355237.6:c.1014A>C	ENSP00000347379.2:p.Pro338=
ENST00000396442.6:c.1014A>C	ENSP00000379719.2:p.Pro338=
ENST00000538151.2:c.261A>C	ENSP00000445940.1:p.Pro87=
NM_001205254.1:c.1014A>C	NP_001192183.1:p.Pro338=
NM_001205255.1:c.261A>C	NP_001192184.1:p.Pro87=
NM_002538.3:c.1014A>C	NP_002529.1:p.Pro338=
XM_017008913.2:c.852A>C	XP_016864402.1:p.Pro284=
XM_017008914.2:c.852A>C	XP_016864403.1:p.Pro284=
NM_001205254.2:c.1014A>C MANE Select	NP_001192183.1:p.Pro338=
NM_002538.4:c.1014A>C	NP_002529.1:p.Pro338=