Canonical Allele Identifier: CA2834824169

Gene: FAM20C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.255775_255776del , CM000669.2:g.255775_255776del	GRCh38
NC_000007.13:g.295741_295742del , CM000669.1:g.295741_295742del	GRCh37
NG_033970.1:g.65411_65412del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313766.6:c.1073-74_1073-73del MANE Select	ENSP00000322323.5:n.1073-74_1073-73del
ENST00000313766.5:c.1073-74_1073-73del	ENSP00000322323.5:n.1073-74_1073-73del
ENST00000515795.1:n.730-74_730-73del
NM_020223.3:c.1073-74_1073-73del	NP_064608.2:n.1073-74_1073-73del
XR_242097.3:n.1220-74_1220-73del
XM_017012450.1:c.1334-74_1334-73del	XP_016867939.1:n.1334-74_1334-73del
XM_017012451.1:c.1331-74_1331-73del	XP_016867940.1:n.1331-74_1331-73del
XM_017012455.2:c.371-74_371-73del	XP_016867944.1:n.371-74_371-73del
NM_020223.4:c.1073-74_1073-73del MANE Select	NP_064608.2:n.1073-74_1073-73del