Canonical Allele Identifier: CA10344186

Gene: FAM9B

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9025541C>T , CM000685.2:g.9025541C>T	GRCh38
NC_000023.10:g.8993582C>T , CM000685.1:g.8993582C>T	GRCh37
NC_000023.9:g.8953582C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_205849.3:c.535G>A MANE Select	NP_995321.1:p.Asp179Asn
ENST00000327220.10:c.535G>A MANE Select	ENSP00000318716.5:p.Asp179Asn
ENST00000327220.9:c.535G>A	ENSP00000318716.5:p.Asp179Asn
ENST00000362066.7:c.655G>A	ENSP00000354770.3:p.Asp219Asn
ENST00000428477.1:c.535G>A	ENSP00000412606.1:p.Asp179Asn
ENST00000461107.5:n.3262G>A
ENST00000472522.5:c.*438G>A	ENSP00000431456.1:n.*438G>A
ENST00000472522.6:c.535G>A	ENSP00000431456.2:p.Asp179Asn
ENST00000651278.1:c.535G>A	ENSP00000498495.1:p.Asp179Asn
XM_011545464.1:c.535G>A	XP_011543766.1:p.Asp179Asn
XM_024452345.1:c.670G>A	XP_024308113.1:p.Asp224Asn
XM_024452346.1:c.535G>A	XP_024308114.1:p.Asp179Asn