LDH info

Canonical Allele Identifier: CA11653016
Gene: FAM13A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10007590

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88995984A>G , CM000666.2:g.88995984A>G GRCh38
NC_000004.11:g.89917135A>G , CM000666.1:g.89917135A>G GRCh37
NC_000004.10:g.90136158A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_014883.3:c.428-4834T>C VV NP_055698.2:p.=
XM_005262681.2:c.428-4834T>C XP_005262738.1:p.=
XM_005262682.2:c.368-4834T>C XP_005262739.1:p.=
XM_005262683.2:c.428-4834T>C XP_005262740.1:p.=
XM_005262684.2:c.-23+24476T>C XP_005262741.1:p.=
XM_011531516.1:c.428-4834T>C XP_011529818.1:p.=
XM_011531517.1:c.428-4834T>C XP_011529819.1:p.=
XM_011531518.1:c.-131-4834T>C XP_011529820.1:p.=
XM_011531519.1:c.-131-4834T>C XP_011529821.1:p.=
XM_011531520.1:c.-23+22906T>C XP_011529822.1:p.=
XM_005262681.3:c.428-4834T>C XP_005262738.1:p.=
XM_005262683.3:c.428-4834T>C XP_005262740.1:p.=
XM_005262684.4:c.-23+24476T>C XP_005262741.1:p.=
XM_011531517.2:c.428-4834T>C XP_011529819.1:p.=
XM_011531519.3:c.-131-4834T>C XP_011529821.1:p.=
XM_017007624.2:c.428-4834T>C XP_016863113.1:p.=
XM_017007625.1:c.263-4834T>C XP_016863114.1:p.=
XM_017007626.1:c.74+22906T>C XP_016863115.1:p.=
XM_017007627.1:c.-23+24476T>C XP_016863116.1:p.=
XM_017007628.2:c.-23+24476T>C XP_016863117.1:p.=
XM_017007629.2:c.-2163-4834T>C XP_016863118.1:p.=
XM_017007630.2:c.-58+24476T>C XP_016863119.1:p.=
XM_017007631.2:c.-2163-4834T>C XP_016863120.1:p.=
XM_017007632.2:c.-58+24476T>C XP_016863121.1:p.=
XM_017007633.2:c.-2226-4834T>C XP_016863122.1:p.=
XM_024453870.1:c.428-4834T>C XP_024309638.1:p.=
NM_014883.4:c.428-4834T>C VV MANE Preferred NP_055698.2:p.=
ENST00000264344.9:c.428-4834T>C ENSP00000264344.5:p.=
ENST00000502459.5:n.886-4834T>C
ENST00000509094.5:c.428-4834T>C ENSP00000426517.1:p.=
ENST00000511976.5:c.-23+24476T>C ENSP00000421914.1:p.=
ENST00000512339.5:c.427+24476T>C ENSP00000423800.1:p.=
ENST00000515600.1:c.428-4834T>C ENSP00000422345.1:p.=