Canonical Allele Identifier: CA15768063
Gene: CNTN1 HGNC NCBI

Linked Data

dbSNP Id: rs1442190

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40971838G>A , CM000674.2:g.40971838G>A GRCh38
NC_000012.11:g.41365640G>A , CM000674.1:g.41365640G>A GRCh37
NC_000012.10:g.39651907G>A NCBI36
NG_012058.2:g.284283G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000547849.6:c.*325G>A ENSP00000448653.1:n.*325G>A
ENST00000551295.7:c.1805-9071G>A MANE Select ENSP00000447006.1:n.1805-9071G>A
ENST00000347616.5:c.1805-9071G>A ENSP00000325660.3:n.1805-9071G>A
ENST00000348761.2:c.1772-9071G>A ENSP00000261160.3:n.1772-9071G>A
ENST00000547702.5:c.*325G>A ENSP00000448004.1:n.*325G>A
ENST00000547849.5:c.*325G>A ENSP00000448653.1:n.*325G>A
ENST00000551295.6:c.1805-9071G>A ENSP00000447006.1:n.1805-9071G>A
NM_001256063.1:c.*325G>A NP_001242992.1:n.*325G>A
NM_001256064.1:c.*325G>A NP_001242993.1:n.*325G>A
NM_001843.3:c.1805-9071G>A NP_001834.2:n.1805-9071G>A
NM_175038.2:c.1772-9071G>A NP_778203.1:n.1772-9071G>A
XM_005268651.1:c.1805-9071G>A XP_005268708.1:n.1805-9071G>A
XM_006719241.1:c.1805-9071G>A XP_006719304.1:n.1805-9071G>A
XM_011537926.1:c.1805-9071G>A XP_011536228.1:n.1805-9071G>A
XM_011537927.1:c.1805-9071G>A XP_011536229.1:n.1805-9071G>A
XM_005268651.2:c.1805-9071G>A XP_005268708.1:n.1805-9071G>A
XM_006719241.2:c.1805-9071G>A XP_006719304.1:n.1805-9071G>A
XM_011537926.3:c.1805-9071G>A XP_011536228.1:n.1805-9071G>A
XM_011537927.2:c.1805-9071G>A XP_011536229.1:n.1805-9071G>A
XM_017018826.2:c.*325G>A XP_016874315.1:n.*325G>A
XM_017018827.2:c.*325G>A XP_016874316.1:n.*325G>A
XM_024448843.1:c.*325G>A XP_024304611.1:n.*325G>A
XR_002957288.1:n.2027-9071G>A
XR_002957289.1:n.2148-9071G>A
XR_002957290.1:n.2395-9071G>A
XR_002957291.1:n.2019-9071G>A
NM_001843.4:c.1805-9071G>A MANE Select NP_001834.2:n.1805-9071G>A
NM_001256063.2:c.*325G>A NP_001242992.1:n.*325G>A
NM_001256064.2:c.*325G>A NP_001242993.1:n.*325G>A