Canonical Allele Identifier: CA410515999

Gene: FTCD

Linked Data

• MyVariant Identifiers: chr21:g.47570037C>A (hg19) ; chr21:g.46150123C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46150123C>A , CM000683.2:g.46150123C>A	GRCh38
NC_000021.8:g.47570037C>A , CM000683.1:g.47570037C>A	GRCh37
NC_000021.7:g.46394465C>A	NCBI36
NG_016191.1:g.10445G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397746.8:c.902G>T MANE Select	ENSP00000380854.3:p.Arg301Met
ENST00000291670.9:c.902G>T	ENSP00000291670.5:p.Arg301Met
ENST00000397743.1:c.902G>T	ENSP00000380851.1:p.Arg301Met
ENST00000397746.7:c.902G>T	ENSP00000380854.3:p.Arg301Met
ENST00000397748.5:c.902G>T	ENSP00000380856.1:p.Arg301Met
ENST00000498355.6:n.971G>T
NM_006657.2:c.902G>T	NP_006648.1:p.Arg301Met
NM_206965.1:c.902G>T	NP_996848.1:p.Arg301Met
XM_006723961.2:c.1022G>T	XP_006724024.2:p.Arg341Met
XM_006723962.2:c.1022G>T	XP_006724025.2:p.Arg341Met
XM_011529434.1:c.1022G>T	XP_011527736.1:p.Arg341Met
XM_011529435.1:c.1022G>T	XP_011527737.1:p.Arg341Met
XM_011529436.1:c.1022G>T	XP_011527738.1:p.Arg341Met
XM_011529437.1:c.1022G>T	XP_011527739.1:p.Arg341Met
XM_011529438.1:c.1022G>T	XP_011527740.1:p.Arg341Met
XM_011529439.1:c.509G>T	XP_011527741.1:p.Arg170Met
XM_011529440.1:c.1022G>T	XP_011527742.1:p.Arg341Met
XR_937433.1:n.1205G>T
NM_001320412.1:c.902G>T	NP_001307341.1:p.Arg301Met
XM_006723961.4:c.1022G>T	XP_006724024.2:p.Arg341Met
XM_006723962.4:c.1022G>T	XP_006724025.2:p.Arg341Met
XM_011529434.3:c.1022G>T	XP_011527736.1:p.Arg341Met
XM_011529435.3:c.1022G>T	XP_011527737.1:p.Arg341Met
XM_011529436.3:c.1022G>T	XP_011527738.1:p.Arg341Met
XM_011529437.3:c.1022G>T	XP_011527739.1:p.Arg341Met
XM_011529439.2:c.509G>T	XP_011527741.1:p.Arg170Met
XM_011529440.3:c.1022G>T	XP_011527742.1:p.Arg341Met
XR_937433.3:n.1239G>T
NM_206965.2:c.902G>T MANE Select	NP_996848.1:p.Arg301Met
NM_001320412.2:c.902G>T	NP_001307341.1:p.Arg301Met
NM_006657.3:c.902G>T	NP_006648.1:p.Arg301Met