Canonical Allele Identifier: CA479274914

Gene: CNTN1

Linked Data

• MyVariant Identifiers: chr12:g.41337432C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40943630C>T , CM000674.2:g.40943630C>T	GRCh38
NC_000012.11:g.41337432C>T , CM000674.1:g.41337432C>T	GRCh37
NC_000012.10:g.39623699C>T	NCBI36
NG_012058.2:g.256075C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000547849.6:c.1413C>T	ENSP00000448653.1:p.Ile471=
ENST00000551295.7:c.1413C>T MANE Select	ENSP00000447006.1:p.Ile471=
ENST00000347616.5:c.1413C>T	ENSP00000325660.3:p.Ile471=
ENST00000348761.2:c.1380C>T	ENSP00000261160.3:p.Ile460=
ENST00000547702.5:c.1413C>T	ENSP00000448004.1:p.Ile471=
ENST00000547849.5:c.1413C>T	ENSP00000448653.1:p.Ile471=
ENST00000551295.6:c.1413C>T	ENSP00000447006.1:p.Ile471=
NM_001256063.1:c.1413C>T	NP_001242992.1:p.Ile471=
NM_001256064.1:c.1413C>T	NP_001242993.1:p.Ile471=
NM_001843.3:c.1413C>T	NP_001834.2:p.Ile471=
NM_175038.2:c.1380C>T	NP_778203.1:p.Ile460=
XM_005268651.1:c.1413C>T	XP_005268708.1:p.Ile471=
XM_006719241.1:c.1413C>T	XP_006719304.1:p.Ile471=
XM_011537926.1:c.1413C>T	XP_011536228.1:p.Ile471=
XM_011537927.1:c.1413C>T	XP_011536229.1:p.Ile471=
XM_005268651.2:c.1413C>T	XP_005268708.1:p.Ile471=
XM_006719241.2:c.1413C>T	XP_006719304.1:p.Ile471=
XM_011537926.3:c.1413C>T	XP_011536228.1:p.Ile471=
XM_011537927.2:c.1413C>T	XP_011536229.1:p.Ile471=
XM_017018826.2:c.1413C>T	XP_016874315.1:p.Ile471=
XM_017018827.2:c.1413C>T	XP_016874316.1:p.Ile471=
XM_024448843.1:c.1413C>T	XP_024304611.1:p.Ile471=
XR_002957288.1:n.1635C>T
XR_002957289.1:n.1756C>T
XR_002957290.1:n.2003C>T
XR_002957291.1:n.1627C>T
NM_001843.4:c.1413C>T MANE Select	NP_001834.2:p.Ile471=
NM_001256063.2:c.1413C>T	NP_001242992.1:p.Ile471=
NM_001256064.2:c.1413C>T	NP_001242993.1:p.Ile471=