Canonical Allele Identifier: CA2654977149

Gene: FTCD

Linked Data

• gnomAD v4: 21-46138636-CCGCCGTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138641_46138647del , CM000683.2:g.46138641_46138647del	GRCh38
NC_000021.8:g.47558555_47558561del , CM000683.1:g.47558555_47558561del	GRCh37
NC_000021.7:g.46382983_46382989del	NCBI36
NG_016191.1:g.21925_21931del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-157_-151del
ENST00000494498.2:c.42_48del
ENST00000397746.8:c.1308_1314del
ENST00000291670.9:c.1308_1314del
ENST00000397743.1:c.1264_1270del
ENST00000397746.7:c.1308_1314del
ENST00000397748.5:c.1308_1314del
ENST00000460011.5:n.637_643del
ENST00000488577.1:n.334_340del
ENST00000494498.1:n.609_615del
ENST00000498355.6:n.1377_1383del
NM_006657.2:c.1308_1314del
NM_206965.1:c.1308_1314del
XM_006723961.2:c.1557_1563del
XM_006723962.2:c.1557_1563del
XM_011529434.1:c.1557_1563del
XM_011529435.1:c.1428_1434del
XM_011529436.1:c.1557_1563del
XM_011529437.1:c.1557_1563del
XM_011529438.1:c.1428_1434del
XM_011529439.1:c.1044_1050del
XR_937433.1:n.1740_1746del
NM_001320412.1:c.1308_1314del
XM_006723961.4:c.1557_1563del
XM_006723962.4:c.1557_1563del
XM_011529434.3:c.1557_1563del
XM_011529435.3:c.1428_1434del
XM_011529436.3:c.1557_1563del
XM_011529437.3:c.1557_1563del
XM_011529439.2:c.1044_1050del
XR_937433.3:n.1774_1780del
NM_206965.2:c.1308_1314del
NM_001320412.2:c.1308_1314del
NM_006657.3:c.1308_1314del