Canonical Allele Identifier: CA2352626

Gene: FYCO1 CXCR6

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45947552T>G , CM000665.2:g.45947552T>G	GRCh38
NC_000003.11:g.45989044T>G , CM000665.1:g.45989044T>G	GRCh37
NC_000003.10:g.45964048T>G	NCBI36
NG_031955.1:g.53273A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296137.7:c.3944+7697A>C (FYCO1) MANE Select	ENSP00000296137.2:n.3944+7697A>C
ENST00000304552.5:c.*42T>G (CXCR6) MANE Select	ENSP00000304414.4:n.*42T>G
ENST00000296137.6:c.3944+7697A>C (FYCO1)	ENSP00000296137.2:n.3944+7697A>C
ENST00000304552.4:c.*42T>G (CXCR6)	ENSP00000304414.4:n.*42T>G
ENST00000433878.5:c.310+7697A>C (FYCO1)
ENST00000438446.1:c.-44+7697A>C (FYCO1)	ENSP00000398517.1:n.-44+7697A>C
ENST00000438735.1:c.*42T>G (CXCR6)	ENSP00000396218.1:n.*42T>G
ENST00000458629.1:c.*42T>G (CXCR6)	ENSP00000395704.1:n.*42T>G
ENST00000535325.5:c.3944+7697A>C (FYCO1)	ENSP00000441178.1:n.3944+7697A>C
NM_006564.1:c.*42T>G (CXCR6)	NP_006555.1:n.*42T>G
NM_024513.3:c.3944+7697A>C (FYCO1)	NP_078789.2:n.3944+7697A>C
XM_005264809.2:c.*42T>G (CXCR6)	XP_005264866.1:n.*42T>G
XM_006713333.2:c.3944+7697A>C (FYCO1)	XP_006713396.1:n.3944+7697A>C
XM_006713334.2:c.3944+7697A>C (FYCO1)	XP_006713397.1:n.3944+7697A>C
XM_011533290.1:c.*42T>G (CXCR6)	XP_011531592.1:n.*42T>G
XM_011533291.1:c.*42T>G (CXCR6)	XP_011531593.1:n.*42T>G
XM_011534111.1:c.3944+7697A>C (FYCO1)	XP_011532413.1:n.3944+7697A>C
XM_011534112.1:c.3944+7697A>C (FYCO1)	XP_011532414.1:n.3944+7697A>C
XR_245157.1:n.4159+7697A>C (FYCO1)
XM_006713333.3:c.3944+7697A>C (FYCO1)	XP_006713396.1:n.3944+7697A>C
XM_006713334.3:c.3944+7697A>C (FYCO1)	XP_006713397.1:n.3944+7697A>C
XM_011533290.2:c.*42T>G (CXCR6)	XP_011531592.1:n.*42T>G
XM_011533291.2:c.*42T>G (CXCR6)	XP_011531593.1:n.*42T>G
XM_011534111.3:c.3944+7697A>C (FYCO1)	XP_011532413.1:n.3944+7697A>C
XR_001740265.1:n.4040+7697A>C (FYCO1)
NM_006564.2:c.*42T>G (CXCR6) MANE Select	NP_006555.1:n.*42T>G
NM_024513.4:c.3944+7697A>C (FYCO1) MANE Select	NP_078789.2:n.3944+7697A>C
NM_001386421.1:c.3944+7697A>C (FYCO1)	NP_001373350.1:n.3944+7697A>C
NM_001386422.1:c.3944+7697A>C (FYCO1)	NP_001373351.1:n.3944+7697A>C
NM_001386423.1:c.3941+7697A>C (FYCO1)	NP_001373352.1:n.3941+7697A>C
NM_001386424.1:c.3944+7697A>C (FYCO1)	NP_001373353.1:n.3944+7697A>C
NM_001386425.1:c.3944+7697A>C (FYCO1)	NP_001373354.1:n.3944+7697A>C
NM_001386426.1:c.3824+7697A>C (FYCO1)	NP_001373355.1:n.3824+7697A>C
NM_001386427.1:c.3800+7697A>C (FYCO1)	NP_001373356.1:n.3800+7697A>C
NM_001386428.1:c.3944+7697A>C (FYCO1)	NP_001373357.1:n.3944+7697A>C
NM_001386429.1:c.3944+7697A>C (FYCO1)	NP_001373358.1:n.3944+7697A>C
NM_001386430.1:c.3344+7697A>C (FYCO1)	NP_001373359.1:n.3344+7697A>C
NM_001386435.1:c.*42T>G (CXCR6)	NP_001373364.1:n.*42T>G
NM_001386436.1:c.*42T>G (CXCR6)	NP_001373365.1:n.*42T>G
NM_001386437.1:c.*42T>G (CXCR6)	NP_001373366.1:n.*42T>G
NR_170107.1:n.4159+7697A>C (FYCO1)