Canonical Allele Identifier: CA862065263
Gene: FOCAD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.20778632A>T , CM000671.2:g.20778632A>T GRCh38
NC_000009.11:g.20778631A>T , CM000671.1:g.20778631A>T GRCh37
NC_000009.10:g.20768631A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000338382.11:c.907-49A>T MANE Select ENSP00000344307.6:n.907-49A>T
ENST00000338382.10:c.907-49A>T ENSP00000344307.6:n.907-49A>T
ENST00000380249.5:c.907-49A>T ENSP00000369599.1:n.907-49A>T
NM_017794.4:c.907-49A>T NP_060264.4:n.907-49A>T
XM_005251494.3:c.907-49A>T XP_005251551.2:n.907-49A>T
XM_011517944.1:c.907-49A>T XP_011516246.1:n.907-49A>T
XM_011517945.1:c.802-49A>T XP_011516247.1:n.802-49A>T
XM_011517946.1:c.907-49A>T XP_011516248.1:n.907-49A>T
XM_011517947.1:c.907-49A>T XP_011516249.1:n.907-49A>T
XM_011517948.1:c.907-49A>T XP_011516250.1:n.907-49A>T
XM_005251494.4:c.907-49A>T XP_005251551.2:n.907-49A>T
XM_011517945.2:c.802-49A>T XP_011516247.1:n.802-49A>T
XM_017014852.1:c.988-49A>T XP_016870341.1:n.988-49A>T
XM_017014853.1:c.988-49A>T XP_016870342.1:n.988-49A>T
XM_017014854.1:c.883-49A>T XP_016870343.1:n.883-49A>T
XM_017014855.1:c.988-49A>T XP_016870344.1:n.988-49A>T
XM_017014856.1:c.988-49A>T XP_016870345.1:n.988-49A>T
XM_017014857.2:c.907-49A>T XP_016870346.1:n.907-49A>T
XM_017014858.2:c.802-49A>T XP_016870347.1:n.802-49A>T
XM_017014859.1:c.388-49A>T XP_016870348.1:n.388-49A>T
XM_024447585.1:c.907-49A>T XP_024303353.1:n.907-49A>T
XM_024447586.1:c.592-49A>T XP_024303354.1:n.592-49A>T
NM_001375567.1:c.907-49A>T MANE Select NP_001362496.1:n.907-49A>T
NM_001375568.1:c.907-49A>T NP_001362497.1:n.907-49A>T
NM_001375570.1:c.802-49A>T NP_001362499.1:n.802-49A>T
NM_017794.5:c.907-49A>T NP_060264.4:n.907-49A>T
Search 100 bp 5'
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