Canonical Allele Identifier: CA4108893

Gene: FAM20C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.193451C>A , CM000669.2:g.193451C>A	GRCh38
NC_000007.13:g.193451C>A , CM000669.1:g.193451C>A	GRCh37
NC_000007.12:g.288534C>A	NCBI36
NG_033970.1:g.5483C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313766.6:c.252C>A MANE Select	ENSP00000322323.5:p.Asn84Lys
ENST00000313766.5:c.252C>A	ENSP00000322323.5:p.Asn84Lys
NM_020223.3:c.252C>A	NP_064608.2:p.Asn84Lys
XM_011515457.1:c.252C>A	XP_011513759.1:p.Asn84Lys
XR_242097.3:n.478C>A
XM_017012450.1:c.252C>A	XP_016867939.1:p.Asn84Lys
XM_017012451.1:c.252C>A	XP_016867940.1:p.Asn84Lys
XM_017012452.1:c.252C>A	XP_016867941.1:p.Asn84Lys
XM_017012453.1:c.252C>A	XP_016867942.1:p.Asn84Lys
XM_017012454.1:c.252C>A	XP_016867943.1:p.Asn84Lys
XR_001744837.1:n.478C>A
NM_020223.4:c.252C>A MANE Select	NP_064608.2:p.Asn84Lys