Canonical Allele Identifier: CA1166082964
Gene: FAF1 HGNC NCBI
FAF1-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.50472176T>A , CM000663.2:g.50472176T>A GRCh38
NC_000001.10:g.50937848T>A , CM000663.1:g.50937848T>A GRCh37
NC_000001.9:g.50710436T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000396153.7:c.1869+3288A>T (FAF1) MANE Select ENSP00000379457.2:n.1869+3288A>T
ENST00000371778.5:c.1389+3288A>T (FAF1) ENSP00000360843.5:n.1389+3288A>T
ENST00000396153.6:c.1869+3288A>T (FAF1) ENSP00000379457.2:n.1869+3288A>T
ENST00000494400.5:c.1287+3288A>T (FAF1) ENSP00000434929.1:n.1287+3288A>T
NM_007051.2:c.1869+3288A>T (FAF1) NP_008982.1:n.1869+3288A>T
XR_947329.1:n.2666+920T>A (FAF1-AS1)
XM_017000136.1:c.1542+3288A>T (FAF1) XP_016855625.1:n.1542+3288A>T
XM_024452734.1:c.1845+3288A>T (FAF1) XP_024308502.1:n.1845+3288A>T
XM_024452736.1:c.1542+3288A>T (FAF1) XP_024308504.1:n.1542+3288A>T
NM_007051.3:c.1869+3288A>T (FAF1) MANE Select NP_008982.1:n.1869+3288A>T
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