LDH info

Canonical Allele Identifier: CA13491690
Gene: ACAT1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3741049

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108139200G>A , CM000673.2:g.108139200G>A GRCh38
NC_000011.9:g.108009927G>A , CM000673.1:g.108009927G>A GRCh37
NC_000011.8:g.107515137G>A NCBI36
NG_009888.1:g.22670G>A
NG_009888.2:g.27496G>A

Transcript Alleles

HGVS Amino-acid change
NM_000019.3:c.579+159G>A VV NP_000010.1:p.=
XM_006718834.2:c.309+159G>A XP_006718897.1:p.=
XM_006718835.2:c.309+159G>A XP_006718898.1:p.=
XM_006718835.3:c.309+159G>A XP_006718898.1:p.=
XM_017017681.1:c.309+159G>A XP_016873170.1:p.=
XM_017017682.2:c.201+159G>A XP_016873171.1:p.=
XM_017017683.2:c.201+159G>A XP_016873172.1:p.=
XM_024448511.1:c.309+159G>A XP_024304279.1:p.=
XM_024448512.1:c.309+159G>A XP_024304280.1:p.=
XM_024448513.1:c.309+159G>A XP_024304281.1:p.=
XM_024448514.1:c.309+159G>A XP_024304282.1:p.=
XM_024448515.1:c.309+159G>A XP_024304283.1:p.=
NM_000019.4:c.579+159G>A VV MANE Preferred NP_000010.1:p.=
ENST00000265838.8:c.579+159G>A ENSP00000265838.4:p.=
ENST00000531813.5:c.*52+159G>A ENSP00000435965.1:p.=
ENST00000532792.5:n.74+159G>A
ENST00000534773.1:n.322+159G>A