LDH info

Canonical Allele Identifier: CA168644844
Gene: CNTNAP2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10244837

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.146778222G>A , CM000669.2:g.146778222G>A GRCh38
NC_000007.13:g.146475314G>A , CM000669.1:g.146475314G>A GRCh37
NC_000007.12:g.146106247G>A NCBI36
NG_007092.2:g.666862G>A
NG_007092.3:g.667222G>A

Transcript Alleles

HGVS Amino-acid change
NM_014141.5:c.208+3841G>A VV NP_054860.1:p.=
XM_017011950.2:c.208+3841G>A XP_016867439.1:p.=
NM_014141.6:c.208+3841G>A VV MANE Preferred NP_054860.1:p.=
ENST00000361727.7:c.208+3841G>A ENSP00000354778.3:p.=
ENST00000625365.2:c.208+3841G>A ENSP00000485955.1:p.=