Canonical Allele Identifier: CA2627512336

Gene: FAN1

Linked Data

• gnomAD v4: 15-30905512-TGTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.30905513_30905515del , CM000677.2:g.30905513_30905515del	GRCh38
NC_000015.9:g.31197716_31197718del , CM000677.1:g.31197716_31197718del	GRCh37
NC_000015.8:g.28985008_28985010del	NCBI36
NG_032946.1:g.6662_6664del
NG_032946.2:g.6662_6664del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362065.9:c.850_852del MANE Select	ENSP00000354497.4:p.Val284del
ENST00000561607.6:c.850_852del	ENSP00000454223.1:p.Val284del
ENST00000562892.2:c.-57+923_-57+925del	ENSP00000457680.2:n.-57+923_-57+925del
ENST00000568145.6:n.110+923_110+925del
ENST00000602886.2:n.1027_1029del
ENST00000654013.1:n.1126_1128del
ENST00000654056.1:c.-57+923_-57+925del	ENSP00000499726.1:n.-57+923_-57+925del
ENST00000655421.1:n.1121_1123del
ENST00000656109.1:n.179+923_179+925del
ENST00000656307.1:n.1102_1104del
ENST00000656435.1:c.850_852del	ENSP00000499534.1:p.Val284del
ENST00000657391.1:c.850_852del	ENSP00000499703.1:p.Val284del
ENST00000658773.1:c.850_852del	ENSP00000499742.1:p.Val284del
ENST00000661974.1:c.344_346del
ENST00000662114.1:n.1106_1108del
ENST00000664070.1:c.850_852del	ENSP00000499478.1:p.Val284del
ENST00000664837.1:c.-57+923_-57+925del	ENSP00000499780.1:n.-57+923_-57+925del
ENST00000665705.1:n.1089_1091del
ENST00000665894.1:n.1110_1112del
ENST00000666143.1:c.-229-212_-229-210del	ENSP00000499576.1:n.-229-212_-229-210del
ENST00000666852.1:n.1102_1104del
ENST00000667837.1:n.965+160_965+162del
ENST00000670074.1:c.690+160_690+162del	ENSP00000499252.1:n.690+160_690+162del
ENST00000670849.1:c.850_852del	ENSP00000499638.1:p.Val284del
ENST00000362065.8:c.850_852del	ENSP00000354497.4:p.Val284del
ENST00000561594.5:c.850_852del	ENSP00000455983.1:p.Val284del
ENST00000561607.5:c.850_852del	ENSP00000454223.1:p.Val284del
ENST00000562892.1:c.52+923_52+925del	ENSP00000457680.1:n.52+923_52+925del
ENST00000565280.5:c.850_852del	ENSP00000455573.1:p.Val284del
ENST00000565466.5:c.850_852del	ENSP00000454544.1:p.Val284del
NM_001146094.1:c.850_852del	NP_001139566.1:p.Val284del
NM_001146095.1:c.850_852del	NP_001139567.1:p.Val284del
NM_001146096.1:c.850_852del	NP_001139568.1:p.Val284del
NM_014967.4:c.850_852del	NP_055782.3:p.Val284del
XM_005254232.3:c.850_852del	XP_005254289.1:p.Val284del
XM_005254234.3:c.850_852del	XP_005254291.1:p.Val284del
XM_005254235.3:c.850_852del	XP_005254292.1:p.Val284del
XM_005254236.2:c.850_852del	XP_005254293.1:p.Val284del
XM_011521370.1:c.52+923_52+925del	XP_011519672.1:n.52+923_52+925del
XM_011521371.1:c.-470_-468del	XP_011519673.1:n.-470_-468del
XM_011521372.1:c.850_852del	XP_011519674.1:p.Val284del
XM_005254232.4:c.850_852del	XP_005254289.1:p.Val284del
XM_005254234.5:c.850_852del	XP_005254291.1:p.Val284del
XM_011521370.2:c.52+923_52+925del	XP_011519672.1:n.52+923_52+925del
XM_011521372.2:c.850_852del	XP_011519674.1:p.Val284del
XM_017022012.2:c.-620_-618del	XP_016877501.1:n.-620_-618del
XM_017022013.1:c.-620_-618del	XP_016877502.1:n.-620_-618del
XM_024449874.1:c.-470_-468del	XP_024305642.1:n.-470_-468del
XR_001751149.1:n.1149_1151del
XR_001751151.1:n.1145_1147del
NM_014967.5:c.850_852del MANE Select	NP_055782.3:p.Val284del
NM_001146094.2:c.850_852del	NP_001139566.1:p.Val284del
NM_001146096.2:c.850_852del	NP_001139568.1:p.Val284del