LDH info

Canonical Allele Identifier: CA240400637
Gene: SYT1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10735416

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.79191123T>C , CM000674.2:g.79191123T>C GRCh38
NC_000012.11:g.79584903T>C , CM000674.1:g.79584903T>C GRCh37
NC_000012.10:g.78109034T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001135805.1:c.-17-26380T>C VV NP_001129277.1:p.=
NM_001135806.1:c.-17-26380T>C VV NP_001129278.1:p.=
NM_001291901.1:c.-17-26380T>C VV NP_001278830.1:p.=
NM_005639.2:c.-17-26380T>C VV NP_005630.1:p.=
XM_005269113.2:c.-17-26380T>C XP_005269170.1:p.=
XM_006719576.1:c.-17-26380T>C XP_006719639.1:p.=
XM_011538710.1:c.-17-26380T>C XP_011537012.1:p.=
XM_005269113.3:c.-17-26380T>C XP_005269170.1:p.=
XM_011538710.2:c.-17-26380T>C XP_011537012.1:p.=
NM_005639.3:c.-17-26380T>C VV MANE Preferred NP_005630.1:p.=
ENST00000261205.8:c.-17-26380T>C ENSP00000261205.4:p.=
ENST00000393240.7:c.-17-26380T>C ENSP00000376932.3:p.=
ENST00000446242.3:c.-17-26380T>C ENSP00000401559.2:p.=
ENST00000457153.6:c.-17-26380T>C ENSP00000391056.2:p.=
ENST00000547046.5:c.-17-26380T>C ENSP00000448964.1:p.=
ENST00000549454.5:n.569-26380T>C
ENST00000549671.5:c.-17-26380T>C ENSP00000450321.1:p.=
ENST00000551304.5:c.-17-26380T>C ENSP00000447656.1:p.=
ENST00000552074.5:c.-17-26380T>C ENSP00000447035.1:p.=
ENST00000552624.5:c.-17-26380T>C ENSP00000448861.1:p.=
ENST00000552744.5:c.-17-26380T>C ENSP00000447575.1:p.=