LDH info

Canonical Allele Identifier: CA7019781
Gene: ABCC4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11568658

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.95210754C>A , CM000675.2:g.95210754C>A GRCh38
NC_000013.10:g.95863008C>A , CM000675.1:g.95863008C>A GRCh37
NC_000013.9:g.94661009C>A NCBI36
NG_050651.1:g.95693G>T

Transcript Alleles

HGVS Amino-acid change
NM_001105515.2:c.559G>T VV NP_001098985.1:p.Gly187Trp
NM_001301829.1:c.559G>T VV NP_001288758.1:p.Gly187Trp
NM_001301830.1:c.334G>T VV NP_001288759.1:p.Gly112Trp
NM_005845.4:c.559G>T VV NP_005836.2:p.Gly187Trp
XM_005254025.2:c.430G>T XP_005254082.1:p.Gly144Trp
XM_006719914.1:c.559G>T XP_006719977.1:p.Gly187Trp
XM_011521047.1:c.10G>T XP_011519349.1:p.Gly4Trp
XM_017020319.1:c.430G>T XP_016875808.1:p.Gly144Trp
XM_017020320.2:c.559G>T XP_016875809.1:p.Gly187Trp
XM_017020322.1:c.430G>T XP_016875811.1:p.Gly144Trp
NM_001105515.3:c.559G>T VV NP_001098985.1:p.Gly187Trp
NM_001301829.2:c.559G>T VV NP_001288758.1:p.Gly187Trp
NM_001301830.2:c.334G>T VV NP_001288759.1:p.Gly112Trp
ENST00000376887.8:c.559G>T ENSP00000366084.4:p.Gly187Trp
ENST00000536256.3:c.334G>T ENSP00000442024.1:p.Gly112Trp
ENST00000629385.1:c.559G>T ENSP00000487081.1:p.Gly187Trp