LDH info

Canonical Allele Identifier: CA15767517
Gene: SLCO1C1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3794271

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20707159G>A , CM000674.2:g.20707159G>A GRCh38
NC_000012.11:g.20860093G>A , CM000674.1:g.20860093G>A GRCh37
NC_000012.10:g.20751360G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001145944.1:c.50+1078G>A VV NP_001139416.1:p.=
NM_001145945.1:c.404+1078G>A VV NP_001139417.1:p.=
NM_001145946.1:c.404+1078G>A VV NP_001139418.1:p.=
NM_017435.4:c.404+1078G>A VV NP_059131.1:p.=
XM_005253394.1:c.404+1078G>A XP_005253451.1:p.=
XM_005253396.1:c.50+1078G>A XP_005253453.1:p.=
XM_005253397.2:c.404+1078G>A XP_005253454.1:p.=
XM_011520703.1:c.404+1078G>A XP_011519005.1:p.=
XM_011520704.1:c.404+1078G>A XP_011519006.1:p.=
XM_011520705.1:c.404+1078G>A XP_011519007.1:p.=
XM_011520706.1:c.50+1078G>A XP_011519008.1:p.=
XM_011520707.1:c.50+1078G>A XP_011519009.1:p.=
XM_011520708.1:c.50+1078G>A XP_011519010.1:p.=
XM_011520709.1:c.50+1078G>A XP_011519011.1:p.=
XM_011520710.1:c.404+1078G>A XP_011519012.1:p.=
XM_011520711.1:c.-150+1078G>A XP_011519013.1:p.=
XR_931308.1:n.759+1078G>A
XM_005253394.3:c.404+1078G>A XP_005253451.1:p.=
XM_005253396.3:c.50+1078G>A XP_005253453.1:p.=
XM_011520703.3:c.404+1078G>A XP_011519005.1:p.=
XM_011520704.3:c.404+1078G>A XP_011519006.1:p.=
XM_011520711.3:c.-150+1078G>A XP_011519013.1:p.=
XM_017019486.2:c.50+1078G>A XP_016874975.1:p.=
XM_017019487.2:c.50+1078G>A XP_016874976.1:p.=
XM_017019489.2:c.-307+1078G>A XP_016874978.1:p.=
XM_017019490.2:c.-271+1078G>A XP_016874979.1:p.=
XM_024449024.1:c.50+1078G>A XP_024304792.1:p.=
XM_024449025.1:c.50+1078G>A XP_024304793.1:p.=
XR_001748768.2:n.13817+1078G>A
XR_001748769.2:n.13817+1078G>A
XR_001748770.2:n.13817+1078G>A
XR_001748771.2:n.14314+1078G>A
NM_001145944.2:c.50+1078G>A VV NP_001139416.1:p.=
NM_001145945.2:c.404+1078G>A VV NP_001139417.1:p.=
NM_001145946.2:c.404+1078G>A VV NP_001139418.1:p.=
NM_017435.5:c.404+1078G>A VV MANE Preferred NP_059131.1:p.=
ENST00000266509.6:c.404+1078G>A ENSP00000266509.2:p.=
ENST00000539415.5:c.130-4227G>A ENSP00000437399.1:p.=
ENST00000540354.5:c.404+1078G>A ENSP00000438665.1:p.=
ENST00000545102.1:c.50+1078G>A ENSP00000444527.1:p.=
ENST00000545604.5:c.404+1078G>A ENSP00000444149.1:p.=