Canonical Allele Identifier: CA391524249

Gene: FAN1

Linked Data

• MyVariant Identifiers: chr15:g.31197683A>C (hg19) ; chr15:g.30905480A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.30905480A>C , CM000677.2:g.30905480A>C	GRCh38
NC_000015.9:g.31197683A>C , CM000677.1:g.31197683A>C	GRCh37
NC_000015.8:g.28984975A>C	NCBI36
NG_032946.1:g.6629A>C
NG_032946.2:g.6629A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362065.9:c.817A>C MANE Select	ENSP00000354497.4:p.Asn273His
ENST00000561607.6:c.817A>C	ENSP00000454223.1:p.Asn273His
ENST00000562892.2:c.-57+890A>C	ENSP00000457680.2:n.-57+890A>C
ENST00000568145.6:n.110+890A>C
ENST00000602886.2:n.994A>C
ENST00000654013.1:n.1093A>C
ENST00000654056.1:c.-57+890A>C	ENSP00000499726.1:n.-57+890A>C
ENST00000655421.1:n.1088A>C
ENST00000656109.1:n.179+890A>C
ENST00000656307.1:n.1069A>C
ENST00000656435.1:c.817A>C	ENSP00000499534.1:p.Asn273His
ENST00000657391.1:c.817A>C	ENSP00000499703.1:p.Asn273His
ENST00000658773.1:c.817A>C	ENSP00000499742.1:p.Asn273His
ENST00000661974.1:c.311A>C
ENST00000662114.1:n.1073A>C
ENST00000664070.1:c.817A>C	ENSP00000499478.1:p.Asn273His
ENST00000664837.1:c.-57+890A>C	ENSP00000499780.1:n.-57+890A>C
ENST00000665705.1:n.1056A>C
ENST00000665894.1:n.1077A>C
ENST00000666143.1:c.-229-245A>C	ENSP00000499576.1:n.-229-245A>C
ENST00000666852.1:n.1069A>C
ENST00000667837.1:n.965+127A>C
ENST00000670074.1:c.690+127A>C	ENSP00000499252.1:n.690+127A>C
ENST00000670849.1:c.817A>C	ENSP00000499638.1:p.Asn273His
ENST00000362065.8:c.817A>C	ENSP00000354497.4:p.Asn273His
ENST00000561594.5:c.817A>C	ENSP00000455983.1:p.Asn273His
ENST00000561607.5:c.817A>C	ENSP00000454223.1:p.Asn273His
ENST00000562892.1:c.52+890A>C	ENSP00000457680.1:n.52+890A>C
ENST00000565280.5:c.817A>C	ENSP00000455573.1:p.Asn273His
ENST00000565466.5:c.817A>C	ENSP00000454544.1:p.Asn273His
NM_001146094.1:c.817A>C	NP_001139566.1:p.Asn273His
NM_001146095.1:c.817A>C	NP_001139567.1:p.Asn273His
NM_001146096.1:c.817A>C	NP_001139568.1:p.Asn273His
NM_014967.4:c.817A>C	NP_055782.3:p.Asn273His
XM_005254232.3:c.817A>C	XP_005254289.1:p.Asn273His
XM_005254234.3:c.817A>C	XP_005254291.1:p.Asn273His
XM_005254235.3:c.817A>C	XP_005254292.1:p.Asn273His
XM_005254236.2:c.817A>C	XP_005254293.1:p.Asn273His
XM_011521370.1:c.52+890A>C	XP_011519672.1:n.52+890A>C
XM_011521371.1:c.-503A>C	XP_011519673.1:n.-503A>C
XM_011521372.1:c.817A>C	XP_011519674.1:p.Asn273His
XM_005254232.4:c.817A>C	XP_005254289.1:p.Asn273His
XM_005254234.5:c.817A>C	XP_005254291.1:p.Asn273His
XM_011521370.2:c.52+890A>C	XP_011519672.1:n.52+890A>C
XM_011521372.2:c.817A>C	XP_011519674.1:p.Asn273His
XM_017022012.2:c.-653A>C	XP_016877501.1:n.-653A>C
XM_017022013.1:c.-653A>C	XP_016877502.1:n.-653A>C
XM_024449874.1:c.-503A>C	XP_024305642.1:n.-503A>C
XR_001751149.1:n.1116A>C
XR_001751151.1:n.1112A>C
NM_014967.5:c.817A>C MANE Select	NP_055782.3:p.Asn273His
NM_001146094.2:c.817A>C	NP_001139566.1:p.Asn273His
NM_001146096.2:c.817A>C	NP_001139568.1:p.Asn273His