Canonical Allele Identifier: CA397485154
Community Standard Title: NM_000135.4(FANCA):c.3814C>T (p.His1272Tyr)
Gene: FANCA HGNC NCBI
ZNF276 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89740818G>A , CM000678.2:g.89740818G>A GRCh38
NC_000016.9:g.89807226G>A , CM000678.1:g.89807226G>A GRCh37
NC_000016.8:g.88334727G>A NCBI36
NG_011706.1:g.80840C>T , LRG_495:g.80840C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000135.4:c.3814C>T (FANCA) MANE Select NP_000126.2:p.His1272Tyr
NM_001113525.2:c.*2572G>A (ZNF276) MANE Select NP_001106997.1:n.*2572G>A
ENST00000389301.8:c.3814C>T (FANCA) MANE Select ENSP00000373952.3:p.His1272Tyr
ENST00000443381.7:c.*2572G>A (ZNF276) MANE Select ENSP00000415836.2:n.*2572G>A
NM_000135.2:c.3814C>T , LRG_495t1:c.3814C>T (FANCA) NP_000126.2:p.His1272Tyr
NM_000135.3:c.3814C>T (FANCA) NP_000126.2:p.His1272Tyr
NM_001113525.1:c.*2572G>A (ZNF276) NP_001106997.1:n.*2572G>A
NM_001286167.1:c.3814C>T (FANCA) NP_001273096.1:p.His1272Tyr
NM_001286167.2:c.3814C>T (FANCA) NP_001273096.1:p.His1272Tyr
NM_001286167.3:c.3814C>T (FANCA) NP_001273096.1:p.His1272Tyr
NM_152287.3:c.*2572G>A (ZNF276) NP_689500.2:n.*2572G>A
NM_152287.4:c.*2572G>A (ZNF276) NP_689500.2:n.*2572G>A
NR_110122.2:n.4572G>A (ZNF276)
NR_110126.2:n.4455G>A (ZNF276)
NR_110128.2:n.4395G>A (ZNF276)
NR_110129.2:n.4489G>A (ZNF276)
ENST00000289816.9:c.*2572G>A (ZNF276) ENSP00000289816.5:n.*2572G>A
ENST00000305699.15:n.1057C>T (FANCA)
ENST00000389301.7:c.3814C>T (FANCA) ENSP00000373952.3:p.His1272Tyr
ENST00000561667.2:c.*2292C>T (FANCA) ENSP00000512522.1:n.*2292C>T
ENST00000564475.5:c.144C>T (FANCA)
ENST00000564475.6:c.3814C>T (FANCA) ENSP00000454977.2:p.His1272Tyr
ENST00000564870.1:c.30-719C>T (FANCA)
ENST00000564969.5:n.99C>T (FANCA)
ENST00000567510.2:c.2384C>T (FANCA) ENSP00000455969.1:n.2384C>T
ENST00000567879.5:c.292C>T (FANCA) ENSP00000457006.1:p.His98Tyr
ENST00000568369.5:c.3814C>T (FANCA) ENSP00000456829.1:p.His1272Tyr
ENST00000568369.6:c.3814C>T (FANCA) ENSP00000456829.1:p.His1272Tyr
ENST00000568626.1:c.523C>T (FANCA)
ENST00000696274.1:n.3775C>T (FANCA)
ENST00000696275.1:c.*3049C>T (FANCA) ENSP00000512517.1:n.*3049C>T
ENST00000696286.1:c.3814C>T (FANCA) ENSP00000512523.1:p.His1272Tyr
ENST00000696287.1:c.3685C>T (FANCA) ENSP00000512524.1:p.His1229Tyr
ENST00000696291.1:c.*3246C>T (FANCA) ENSP00000512530.1:n.*3246C>T
XM_005256294.3:c.3814C>T (FANCA) XP_005256351.1:p.His1272Tyr
XM_005256294.4:c.3814C>T (FANCA) XP_005256351.1:p.His1272Tyr
XM_011522945.1:c.3685C>T (FANCA) XP_011521247.1:p.His1229Tyr
XM_011522945.2:c.3685C>T (FANCA) XP_011521247.1:p.His1229Tyr
XM_011522946.1:c.2791C>T (FANCA) XP_011521248.1:p.His931Tyr
XM_011522946.3:c.2791C>T (FANCA) XP_011521248.1:p.His931Tyr
XM_011522947.1:c.2791C>T (FANCA) XP_011521249.1:p.His931Tyr
XM_011522947.2:c.2791C>T (FANCA) XP_011521249.1:p.His931Tyr
XM_017023044.2:c.3685C>T (FANCA) XP_016878533.1:p.His1229Tyr
XM_024450189.1:c.2791C>T (FANCA) XP_024305957.1:p.His931Tyr
XR_001751866.1:n.3684C>T (FANCA)
XR_933244.1:n.3857C>T (FANCA)
XR_933244.2:n.3857C>T (FANCA)
XR_933245.1:n.3718C>T (FANCA)
XR_933245.2:n.3718C>T (FANCA)
XR_933246.1:n.3684C>T (FANCA)