LDH info

Canonical Allele Identifier: CA15176299
Gene: GALNT14 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1000916

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31091689T>C , CM000664.2:g.31091689T>C GRCh38
NC_000002.11:g.31314555T>C , CM000664.1:g.31314555T>C GRCh37
NC_000002.10:g.31168059T>C NCBI36
NG_051040.1:g.52038A>G

Transcript Alleles

HGVS Amino-acid change
NM_001253826.1:c.314+23054A>G VV NP_001240755.1:p.=
NM_001253827.1:c.69+23054A>G VV NP_001240756.1:p.=
NM_024572.3:c.129+46269A>G VV NP_078848.2:p.=
NR_045602.1:n.770-12623A>G
XM_011533104.1:c.315-12623A>G XP_011531406.1:p.=
XM_011533105.1:c.69+23054A>G XP_011531407.1:p.=
XM_011533106.1:c.42+55233A>G XP_011531408.1:p.=
NM_001329095.1:c.-109-12623A>G VV NP_001316024.1:p.=
NM_001329096.1:c.69+23054A>G VV NP_001316025.1:p.=
NM_001329097.1:c.129+46269A>G VV NP_001316026.1:p.=
NM_024572.4:c.129+46269A>G VV MANE Preferred NP_078848.2:p.=
NM_001253826.2:c.314+23054A>G VV NP_001240755.1:p.=
NM_001329095.2:c.-109-12623A>G VV NP_001316024.1:p.=
NM_001329096.2:c.69+23054A>G VV NP_001316025.1:p.=
NM_001329097.2:c.129+46269A>G VV NP_001316026.1:p.=
NM_001253827.2:c.69+23054A>G VV NP_001240756.1:p.=
ENST00000324589.9:c.314+23054A>G ENSP00000314500.5:p.=
ENST00000349752.9:c.129+46269A>G ENSP00000288988.6:p.=
ENST00000406653.5:c.69+23054A>G ENSP00000385435.1:p.=
ENST00000424136.5:n.181+40941A>G
ENST00000430167.1:c.129+46269A>G ENSP00000406399.1:p.=
ENST00000455477.5:n.198+33465A>G
ENST00000461193.5:n.164+33465A>G
ENST00000464038.5:n.388+55233A>G
ENST00000485468.1:n.158-12623A>G
ENST00000490212.5:n.364+37588A>G
ENST00000496397.5:n.202-18514A>G
ENST00000498206.5:n.358+23054A>G