Canonical Allele Identifier: CA366525122

Gene: FAM20C

Linked Data

• MyVariant Identifiers: chr7:g.295848A>T (hg19) ; chr7:g.255882A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.255882A>T , CM000669.2:g.255882A>T	GRCh38
NC_000007.13:g.295848A>T , CM000669.1:g.295848A>T	GRCh37
NG_033970.1:g.65518A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313766.6:c.1106A>T MANE Select	ENSP00000322323.5:p.Tyr369Phe
ENST00000313766.5:c.1106A>T	ENSP00000322323.5:p.Tyr369Phe
ENST00000515795.1:n.763A>T
NM_020223.3:c.1106A>T	NP_064608.2:p.Tyr369Phe
XR_242097.3:n.1253A>T
XM_017012450.1:c.1367A>T	XP_016867939.1:p.Tyr456Phe
XM_017012451.1:c.1364A>T	XP_016867940.1:p.Tyr455Phe
XM_017012455.2:c.404A>T	XP_016867944.1:p.Tyr135Phe
NM_020223.4:c.1106A>T MANE Select	NP_064608.2:p.Tyr369Phe