LDH info

Canonical Allele Identifier: CA13490446
Gene: CNTN5 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10501920

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.99622442C>G , CM000673.2:g.99622442C>G GRCh38
NC_000011.9:g.99493173C>G , CM000673.1:g.99493173C>G GRCh37
NC_000011.8:g.98998383C>G NCBI36
NG_047156.1:g.606467C>G

Transcript Alleles

HGVS Amino-acid change
NM_001243270.1:c.55+66173C>G VV NP_001230199.1:p.=
NM_001243271.1:c.55+66173C>G VV NP_001230200.1:p.=
NM_014361.3:c.55+66173C>G VV NP_055176.1:p.=
NM_175566.2:c.55+66173C>G VV NP_780775.1:p.=
XM_011542871.1:c.55+66173C>G XP_011541173.1:p.=
XM_011542872.1:c.55+66173C>G XP_011541174.1:p.=
XM_011542873.1:c.55+66173C>G XP_011541175.1:p.=
XM_017017926.1:c.55+66173C>G XP_016873415.1:p.=
XM_017017927.1:c.55+66173C>G XP_016873416.1:p.=
XM_017017928.1:c.55+66173C>G XP_016873417.1:p.=
XM_017017929.1:c.55+66173C>G XP_016873418.1:p.=
XR_001747909.1:n.559+66173C>G
NM_014361.4:c.55+66173C>G VV MANE Preferred NP_055176.1:p.=
NM_001243270.2:c.55+66173C>G VV NP_001230199.1:p.=
NM_001243271.2:c.55+66173C>G VV NP_001230200.1:p.=
ENST00000418526.6:c.55+66173C>G ENSP00000393229.2:p.=
ENST00000524871.5:c.55+66173C>G ENSP00000435637.1:p.=
ENST00000527185.5:c.55+66173C>G ENSP00000433575.1:p.=
ENST00000528682.5:c.55+66173C>G ENSP00000436185.1:p.=
ENST00000528727.5:n.559+66173C>G