Canonical Allele Identifier: CA941396593
Gene: CNTN5 HGNC NCBI

Linked Data

dbSNP Id: rs1950977389

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.99622325A>C , CM000673.2:g.99622325A>C GRCh38
NC_000011.9:g.99493056A>C , CM000673.1:g.99493056A>C GRCh37
NC_000011.8:g.98998266A>C NCBI36
NG_047156.1:g.606350A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000524871.6:c.55+66056A>C MANE Select ENSP00000435637.1:n.55+66056A>C
ENST00000418526.6:c.55+66056A>C ENSP00000393229.2:n.55+66056A>C
ENST00000524871.5:c.55+66056A>C ENSP00000435637.1:n.55+66056A>C
ENST00000527185.5:c.55+66056A>C ENSP00000433575.1:n.55+66056A>C
ENST00000528682.5:c.55+66056A>C ENSP00000436185.1:n.55+66056A>C
ENST00000528727.5:n.559+66056A>C
NM_001243270.1:c.55+66056A>C NP_001230199.1:n.55+66056A>C
NM_001243271.1:c.55+66056A>C NP_001230200.1:n.55+66056A>C
NM_014361.3:c.55+66056A>C NP_055176.1:n.55+66056A>C
NM_175566.2:c.55+66056A>C NP_780775.1:n.55+66056A>C
XM_011542871.1:c.55+66056A>C XP_011541173.1:n.55+66056A>C
XM_011542872.1:c.55+66056A>C XP_011541174.1:n.55+66056A>C
XM_011542873.1:c.55+66056A>C XP_011541175.1:n.55+66056A>C
XM_017017926.1:c.55+66056A>C XP_016873415.1:n.55+66056A>C
XM_017017927.1:c.55+66056A>C XP_016873416.1:n.55+66056A>C
XM_017017928.1:c.55+66056A>C XP_016873417.1:n.55+66056A>C
XM_017017929.1:c.55+66056A>C XP_016873418.1:n.55+66056A>C
XR_001747909.1:n.559+66056A>C
NM_014361.4:c.55+66056A>C MANE Select NP_055176.1:n.55+66056A>C
NM_001243270.2:c.55+66056A>C NP_001230199.1:n.55+66056A>C
NM_001243271.2:c.55+66056A>C NP_001230200.1:n.55+66056A>C