Canonical Allele Identifier: CA489642905

Gene: FAN1

Linked Data

• MyVariant Identifiers: chr15:g.31197547T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.30905344T>G , CM000677.2:g.30905344T>G	GRCh38
NC_000015.9:g.31197547T>G , CM000677.1:g.31197547T>G	GRCh37
NC_000015.8:g.28984839T>G	NCBI36
NG_032946.1:g.6493T>G
NG_032946.2:g.6493T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362065.9:c.681T>G MANE Select	ENSP00000354497.4:p.Pro227=
ENST00000561607.6:c.681T>G	ENSP00000454223.1:p.Pro227=
ENST00000562892.2:c.-57+754T>G	ENSP00000457680.2:n.-57+754T>G
ENST00000568145.6:n.110+754T>G
ENST00000602886.2:n.858T>G
ENST00000654013.1:n.957T>G
ENST00000654056.1:c.-57+754T>G	ENSP00000499726.1:n.-57+754T>G
ENST00000655421.1:n.952T>G
ENST00000656109.1:n.179+754T>G
ENST00000656307.1:n.933T>G
ENST00000656435.1:c.681T>G	ENSP00000499534.1:p.Pro227=
ENST00000657391.1:c.681T>G	ENSP00000499703.1:p.Pro227=
ENST00000658773.1:c.681T>G	ENSP00000499742.1:p.Pro227=
ENST00000661974.1:c.175T>G
ENST00000662114.1:n.937T>G
ENST00000664070.1:c.681T>G	ENSP00000499478.1:p.Pro227=
ENST00000664837.1:c.-57+754T>G	ENSP00000499780.1:n.-57+754T>G
ENST00000665705.1:n.920T>G
ENST00000665894.1:n.941T>G
ENST00000666143.1:c.-229-381T>G	ENSP00000499576.1:n.-229-381T>G
ENST00000666852.1:n.933T>G
ENST00000667837.1:n.956T>G
ENST00000670074.1:c.681T>G	ENSP00000499252.1:p.Pro227=
ENST00000670849.1:c.681T>G	ENSP00000499638.1:p.Pro227=
ENST00000362065.8:c.681T>G	ENSP00000354497.4:p.Pro227=
ENST00000561594.5:c.681T>G	ENSP00000455983.1:p.Pro227=
ENST00000561607.5:c.681T>G	ENSP00000454223.1:p.Pro227=
ENST00000562892.1:c.52+754T>G	ENSP00000457680.1:n.52+754T>G
ENST00000565280.5:c.681T>G	ENSP00000455573.1:p.Pro227=
ENST00000565466.5:c.681T>G	ENSP00000454544.1:p.Pro227=
NM_001146094.1:c.681T>G	NP_001139566.1:p.Pro227=
NM_001146095.1:c.681T>G	NP_001139567.1:p.Pro227=
NM_001146096.1:c.681T>G	NP_001139568.1:p.Pro227=
NM_014967.4:c.681T>G	NP_055782.3:p.Pro227=
XM_005254232.3:c.681T>G	XP_005254289.1:p.Pro227=
XM_005254234.3:c.681T>G	XP_005254291.1:p.Pro227=
XM_005254235.3:c.681T>G	XP_005254292.1:p.Pro227=
XM_005254236.2:c.681T>G	XP_005254293.1:p.Pro227=
XM_011521370.1:c.52+754T>G	XP_011519672.1:n.52+754T>G
XM_011521371.1:c.-639T>G	XP_011519673.1:n.-639T>G
XM_011521372.1:c.681T>G	XP_011519674.1:p.Pro227=
XM_005254232.4:c.681T>G	XP_005254289.1:p.Pro227=
XM_005254234.5:c.681T>G	XP_005254291.1:p.Pro227=
XM_011521370.2:c.52+754T>G	XP_011519672.1:n.52+754T>G
XM_011521372.2:c.681T>G	XP_011519674.1:p.Pro227=
XM_017022012.2:c.-789T>G	XP_016877501.1:n.-789T>G
XM_017022013.1:c.-789T>G	XP_016877502.1:n.-789T>G
XM_024449874.1:c.-639T>G	XP_024305642.1:n.-639T>G
XR_001751149.1:n.980T>G
XR_001751151.1:n.976T>G
NM_014967.5:c.681T>G MANE Select	NP_055782.3:p.Pro227=
NM_001146094.2:c.681T>G	NP_001139566.1:p.Pro227=
NM_001146096.2:c.681T>G	NP_001139568.1:p.Pro227=