Canonical Allele Identifier: CA2167723385
Gene: FAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.30905576A= , CM000677.2:g.30905576A= GRCh38
NC_000015.9:g.31197779A= , CM000677.1:g.31197779A= GRCh37
NC_000015.8:g.28985071A= NCBI36
NG_032946.1:g.6725A=
NG_032946.2:g.6725A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362065.9:c.913A= MANE Select ENSP00000354497.4:p.Lys305=
ENST00000561607.6:c.913A= ENSP00000454223.1:p.Lys305=
ENST00000562892.2:c.-57+986A= ENSP00000457680.2:n.-57+986A=
ENST00000568145.6:n.110+986A=
ENST00000602886.2:n.1090A=
ENST00000654013.1:n.1189A=
ENST00000654056.1:c.-57+986A= ENSP00000499726.1:n.-57+986A=
ENST00000655421.1:n.1184A=
ENST00000656109.1:n.179+986A=
ENST00000656307.1:n.1165A=
ENST00000656435.1:c.913A= ENSP00000499534.1:p.Lys305=
ENST00000657391.1:c.913A= ENSP00000499703.1:p.Lys305=
ENST00000658773.1:c.913A= ENSP00000499742.1:p.Lys305=
ENST00000661974.1:c.407A=
ENST00000662114.1:n.1169A=
ENST00000664070.1:c.913A= ENSP00000499478.1:p.Lys305=
ENST00000664837.1:c.-57+986A= ENSP00000499780.1:n.-57+986A=
ENST00000665705.1:n.1152A=
ENST00000665894.1:n.1173A=
ENST00000666143.1:c.-229-149A= ENSP00000499576.1:n.-229-149A=
ENST00000666852.1:n.1165A=
ENST00000667837.1:n.965+223A=
ENST00000670074.1:c.690+223A= ENSP00000499252.1:n.690+223A=
ENST00000670849.1:c.913A= ENSP00000499638.1:p.Lys305=
ENST00000362065.8:c.913A= ENSP00000354497.4:p.Lys305=
ENST00000561594.5:c.913A= ENSP00000455983.1:p.Lys305=
ENST00000561607.5:c.913A= ENSP00000454223.1:p.Lys305=
ENST00000562892.1:c.52+986A= ENSP00000457680.1:n.52+986A=
ENST00000565280.5:c.913A= ENSP00000455573.1:p.Lys305=
ENST00000565466.5:c.913A= ENSP00000454544.1:p.Lys305=
NM_001146094.1:c.913A= NP_001139566.1:p.Lys305=
NM_001146095.1:c.913A= NP_001139567.1:p.Lys305=
NM_001146096.1:c.913A= NP_001139568.1:p.Lys305=
NM_014967.4:c.913A= NP_055782.3:p.Lys305=
XM_005254232.3:c.913A= XP_005254289.1:p.Lys305=
XM_005254234.3:c.913A= XP_005254291.1:p.Lys305=
XM_005254235.3:c.913A= XP_005254292.1:p.Lys305=
XM_005254236.2:c.913A= XP_005254293.1:p.Lys305=
XM_011521370.1:c.52+986A= XP_011519672.1:n.52+986A=
XM_011521371.1:c.-407A= XP_011519673.1:n.-407A=
XM_011521372.1:c.913A= XP_011519674.1:p.Lys305=
XM_005254232.4:c.913A= XP_005254289.1:p.Lys305=
XM_005254234.5:c.913A= XP_005254291.1:p.Lys305=
XM_011521370.2:c.52+986A= XP_011519672.1:n.52+986A=
XM_011521372.2:c.913A= XP_011519674.1:p.Lys305=
XM_017022012.2:c.-557A= XP_016877501.1:n.-557A=
XM_017022013.1:c.-557A= XP_016877502.1:n.-557A=
XM_024449874.1:c.-407A= XP_024305642.1:n.-407A=
XR_001751149.1:n.1212A=
XR_001751151.1:n.1208A=
NM_014967.5:c.913A= MANE Select NP_055782.3:p.Lys305=
NM_001146094.2:c.913A= NP_001139566.1:p.Lys305=
NM_001146096.2:c.913A= NP_001139568.1:p.Lys305=