LDH info

Canonical Allele Identifier: CA15263897
Gene: MCCC1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10513789

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183042285T>G , CM000665.2:g.183042285T>G GRCh38
NC_000003.11:g.182760073T>G , CM000665.1:g.182760073T>G GRCh37
NC_000003.10:g.184242767T>G NCBI36
NG_008100.1:g.62293A>C

Transcript Alleles

HGVS Amino-acid change
NM_001293273.1:c.733-535A>C VV NP_001280202.1:p.=
NM_020166.4:c.1084-535A>C VV NP_064551.3:p.=
NR_120639.1:n.998-535A>C
NR_120640.1:n.1751-535A>C
XM_006713702.1:c.757-535A>C XP_006713765.1:p.=
XM_011512992.1:c.970-535A>C XP_011511294.1:p.=
XM_011512993.1:c.1084-535A>C XP_011511295.1:p.=
XR_241502.2:n.1231-535A>C
XR_924159.1:n.1231-535A>C
NM_001363880.1:c.757-535A>C VV NP_001350809.1:p.=
XM_011512992.2:c.970-535A>C XP_011511294.1:p.=
XR_001740207.2:n.1207-535A>C
XR_001740208.2:n.1207-535A>C
XR_001740209.2:n.1177-535A>C
XR_001740210.1:n.1037-535A>C
XR_002959553.1:n.1207-535A>C
XR_002959554.1:n.1207-535A>C
XR_241502.3:n.1177-535A>C
NM_020166.5:c.1084-535A>C VV MANE Preferred NP_064551.3:p.=
ENST00000265594.8:c.1084-535A>C ENSP00000265594.4:p.=
ENST00000476176.5:c.943-535A>C ENSP00000420433.1:p.=
ENST00000492597.5:c.757-535A>C ENSP00000419898.1:p.=
ENST00000495767.5:c.*665-535A>C ENSP00000419658.1:p.=
ENST00000497830.5:c.*681-535A>C ENSP00000420088.1:p.=
ENST00000497959.5:c.970-535A>C ENSP00000420648.1:p.=
ENST00000539926.5:c.634-535A>C ENSP00000441253.2:p.=
ENST00000610757.4:c.634-535A>C ENSP00000480435.1:p.=
ENST00000629669.2:c.970-535A>C ENSP00000486824.1:p.=