LDH info

Canonical Allele Identifier: CA15165370
Gene: ZNF638 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs6745907

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71381943A>G , CM000664.2:g.71381943A>G GRCh38
NC_000002.11:g.71609073A>G , CM000664.1:g.71609073A>G GRCh37
NC_000002.10:g.71462581A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001014972.2:c.2377+1378A>G VV NP_001014972.1:p.=
NM_001252612.1:c.2377+1378A>G VV NP_001239541.1:p.=
NM_001252613.1:c.2377+1378A>G VV NP_001239542.1:p.=
NM_014497.4:c.2377+1378A>G VV NP_055312.2:p.=
XM_005264263.1:c.844+1378A>G XP_005264320.1:p.=
XM_006711989.1:c.844+1378A>G XP_006712052.1:p.=
XM_011532767.1:c.2377+1378A>G XP_011531069.1:p.=
XM_011532768.1:c.2377+1378A>G XP_011531070.1:p.=
XM_011532769.1:c.2377+1378A>G XP_011531071.1:p.=
XR_939678.1:n.2492+1378A>G
XM_011532768.3:c.2695+1378A>G XP_011531070.2:p.=
XM_017003809.2:c.2695+1378A>G XP_016859298.1:p.=
XM_017003810.2:c.2377+1378A>G XP_016859299.1:p.=
XM_017003812.2:c.2695+1378A>G XP_016859301.1:p.=
XR_001738706.2:n.2741+1378A>G
XR_001738707.2:n.2679+1378A>G
XR_002959264.1:n.2741+1378A>G
XR_002959265.1:n.2741+1378A>G
XR_002959266.1:n.2741+1378A>G
XR_939678.3:n.2741+1378A>G
NM_014497.5:c.2377+1378A>G VV MANE Preferred NP_055312.2:p.=
ENST00000264447.8:c.2377+1378A>G ENSP00000264447.4:p.=
ENST00000409544.5:c.2377+1378A>G ENSP00000386433.1:p.=
ENST00000410075.5:c.2377+1378A>G ENSP00000485608.1:p.=
ENST00000491843.2:n.224+1040A>G