Canonical Allele Identifier: CA397486206
Community Standard Title: NM_000135.4(FANCA):c.3335T>G (p.Val1112Gly)
Gene: FANCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89748672A>C , CM000678.2:g.89748672A>C GRCh38
NC_000016.9:g.89815080A>C , CM000678.1:g.89815080A>C GRCh37
NC_000016.8:g.88342581A>C NCBI36
NG_011706.1:g.72986T>G , LRG_495:g.72986T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000135.4:c.3335T>G MANE Select NP_000126.2:p.Val1112Gly
ENST00000389301.8:c.3335T>G MANE Select ENSP00000373952.3:p.Val1112Gly
NM_000135.2:c.3335T>G , LRG_495t1:c.3335T>G NP_000126.2:p.Val1112Gly
NM_000135.3:c.3335T>G NP_000126.2:p.Val1112Gly
NM_001286167.1:c.3335T>G NP_001273096.1:p.Val1112Gly
NM_001286167.2:c.3335T>G NP_001273096.1:p.Val1112Gly
NM_001286167.3:c.3335T>G NP_001273096.1:p.Val1112Gly
ENST00000305699.15:n.578T>G
ENST00000389301.7:c.3335T>G ENSP00000373952.3:p.Val1112Gly
ENST00000561660.1:c.539T>G
ENST00000561667.2:c.*1813T>G ENSP00000512522.1:n.*1813T>G
ENST00000564475.6:c.3335T>G ENSP00000454977.2:p.Val1112Gly
ENST00000567510.2:c.1905T>G ENSP00000455969.1:n.1905T>G
ENST00000567988.5:c.587T>G
ENST00000568369.5:c.3335T>G ENSP00000456829.1:p.Val1112Gly
ENST00000568369.6:c.3335T>G ENSP00000456829.1:p.Val1112Gly
ENST00000568626.1:c.183T>G
ENST00000568983.5:n.163T>G
ENST00000568983.6:n.354T>G
ENST00000696274.1:n.3296T>G
ENST00000696275.1:c.*2570T>G ENSP00000512517.1:n.*2570T>G
ENST00000696286.1:c.3335T>G ENSP00000512523.1:p.Val1112Gly
ENST00000696287.1:c.3206T>G ENSP00000512524.1:p.Val1069Gly
ENST00000696291.1:c.*2767T>G ENSP00000512530.1:n.*2767T>G
XM_005256294.3:c.3335T>G XP_005256351.1:p.Val1112Gly
XM_005256294.4:c.3335T>G XP_005256351.1:p.Val1112Gly
XM_011522945.1:c.3206T>G XP_011521247.1:p.Val1069Gly
XM_011522945.2:c.3206T>G XP_011521247.1:p.Val1069Gly
XM_011522946.1:c.2312T>G XP_011521248.1:p.Val771Gly
XM_011522946.3:c.2312T>G XP_011521248.1:p.Val771Gly
XM_011522947.1:c.2312T>G XP_011521249.1:p.Val771Gly
XM_011522947.2:c.2312T>G XP_011521249.1:p.Val771Gly
XM_017023044.2:c.3206T>G XP_016878533.1:p.Val1069Gly
XM_024450189.1:c.2312T>G XP_024305957.1:p.Val771Gly
XR_001751866.1:n.3205T>G
XR_933244.1:n.3378T>G
XR_933244.2:n.3378T>G
XR_933245.1:n.3378T>G
XR_933245.2:n.3378T>G
XR_933246.1:n.3205T>G