LDH info

Canonical Allele Identifier: CA3737986
Gene: AGER HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3134940

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32182039T>C , CM000668.2:g.32182039T>C GRCh38
NC_000006.11:g.32149816T>C , CM000668.1:g.32149816T>C GRCh37
NC_000006.10:g.32257794T>C NCBI36
NG_029868.1:g.7284A>G

Transcript Alleles

HGVS Amino-acid change
NM_001136.4:c.964+208A>G VV NP_001127.1:p.=
NM_001206929.1:c.1012+208A>G VV NP_001193858.1:p.=
NM_001206932.1:c.922+208A>G VV NP_001193861.1:p.=
NM_001206934.1:c.1012+208A>G VV NP_001193863.1:p.=
NM_001206936.1:c.912+208A>G VV NP_001193865.1:p.=
NM_001206940.1:c.964+208A>G VV NP_001193869.1:p.=
NM_001206954.1:c.823-407A>G VV NP_001193883.1:p.=
NM_001206966.1:c.964+208A>G VV NP_001193895.1:p.=
NM_172197.2:c.810-407A>G VV NP_751947.1:p.=
NR_038190.1:n.1247+208A>G
XM_017010328.2:c.964-407A>G XP_016865817.1:p.=
XR_001743189.2:n.1029-407A>G
XR_001743190.2:n.981-407A>G
NM_001136.5:c.964+208A>G VV MANE Preferred NP_001127.1:p.=
NM_001206932.2:c.922+208A>G VV NP_001193861.1:p.=
NM_001206936.2:c.912+208A>G VV NP_001193865.1:p.=
NM_001206940.2:c.964+208A>G VV NP_001193869.1:p.=
NM_001206954.2:c.823-407A>G VV NP_001193883.1:p.=
NM_001206966.2:c.964+208A>G VV NP_001193895.1:p.=
NM_172197.3:c.810-407A>G VV NP_751947.1:p.=
NR_038190.2:n.1178+208A>G
ENST00000375055.6:c.964+208A>G ENSP00000364195.2:p.=
ENST00000375065.6:c.151+208A>G ENSP00000364206.6:p.=
ENST00000375067.7:c.810-407A>G ENSP00000364208.3:p.=
ENST00000375069.7:c.1012+208A>G ENSP00000364210.4:p.=
ENST00000375070.7:c.661+208A>G ENSP00000364211.4:p.=
ENST00000375076.8:c.964+208A>G ENSP00000364217.4:p.=
ENST00000438221.6:c.1012+208A>G ENSP00000387887.2:p.=
ENST00000473619.5:n.506+208A>G
ENST00000484849.5:n.1171+208A>G
ENST00000488669.5:n.506+208A>G
ENST00000620802.4:c.283-606A>G ENSP00000484081.1:p.=