Canonical Allele Identifier: CA4108976

Gene: FAM20C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.195679C>T , CM000669.2:g.195679C>T	GRCh38
NC_000007.13:g.195679C>T , CM000669.1:g.195679C>T	GRCh37
NC_000007.12:g.290762C>T	NCBI36
NG_033970.1:g.7711C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020223.4:c.731C>T MANE Select	NP_064608.2:p.Pro244Leu
ENST00000313766.6:c.731C>T MANE Select	ENSP00000322323.5:p.Pro244Leu
NM_020223.3:c.731C>T	NP_064608.2:p.Pro244Leu
ENST00000313766.5:c.731C>T	ENSP00000322323.5:p.Pro244Leu
ENST00000471328.1:n.55C>T
ENST00000477004.1:n.212C>T
XM_011515457.1:c.731C>T	XP_011513759.1:p.Pro244Leu
XM_017012450.1:c.731C>T	XP_016867939.1:p.Pro244Leu
XM_017012451.1:c.731C>T	XP_016867940.1:p.Pro244Leu
XM_017012452.1:c.731C>T	XP_016867941.1:p.Pro244Leu
XM_017012453.1:c.731C>T	XP_016867942.1:p.Pro244Leu
XM_017012454.1:c.731C>T	XP_016867943.1:p.Pro244Leu
XR_001744837.1:n.957C>T
XR_242097.3:n.957C>T