Canonical Allele Identifier: CA4108920

Gene: FAM20C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.193799G>C , CM000669.2:g.193799G>C	GRCh38
NC_000007.13:g.193799G>C , CM000669.1:g.193799G>C	GRCh37
NC_000007.12:g.288882G>C	NCBI36
NG_033970.1:g.5831G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020223.4:c.600G>C MANE Select	NP_064608.2:p.Pro200=
ENST00000313766.6:c.600G>C MANE Select	ENSP00000322323.5:p.Pro200=
NM_020223.3:c.600G>C	NP_064608.2:p.Pro200=
ENST00000313766.5:c.600G>C	ENSP00000322323.5:p.Pro200=
XM_011515457.1:c.600G>C	XP_011513759.1:p.Pro200=
XM_017012450.1:c.600G>C	XP_016867939.1:p.Pro200=
XM_017012451.1:c.600G>C	XP_016867940.1:p.Pro200=
XM_017012452.1:c.600G>C	XP_016867941.1:p.Pro200=
XM_017012453.1:c.600G>C	XP_016867942.1:p.Pro200=
XM_017012454.1:c.600G>C	XP_016867943.1:p.Pro200=
XR_001744837.1:n.826G>C
XR_242097.3:n.826G>C