Canonical Allele Identifier: CA360448741

Gene: FAM81B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.95428719A>C , CM000667.2:g.95428719A>C	GRCh38
NC_000005.9:g.94764423A>C , CM000667.1:g.94764423A>C	GRCh37
NC_000005.8:g.94790179A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_152548.3:c.773A>C MANE Select	NP_689761.2:p.Asn258Thr
ENST00000283357.10:c.773A>C MANE Select	ENSP00000283357.5:p.Asn258Thr
NM_152548.2:c.773A>C	NP_689761.2:p.Asn258Thr
ENST00000283357.9:c.773A>C	ENSP00000283357.5:p.Asn258Thr
ENST00000503099.1:c.554A>C
ENST00000503361.5:c.492A>C	ENSP00000424883.1:n.492A>C
ENST00000507832.5:c.762A>C
ENST00000512365.1:c.41A>C	ENSP00000421181.1:p.Asn14Thr
ENST00000513529.5:c.492A>C
XM_005271905.2:c.215A>C	XP_005271962.2:p.Asn72Thr
XM_005271906.3:c.161A>C	XP_005271963.2:p.Asn54Thr
XM_011543207.1:c.773A>C	XP_011541509.1:p.Asn258Thr
XM_011543208.1:c.773A>C	XP_011541510.1:p.Asn258Thr
XM_011543209.1:c.485A>C	XP_011541511.1:p.Asn162Thr
XM_011543209.2:c.485A>C	XP_011541511.1:p.Asn162Thr
XM_011543210.1:c.215A>C	XP_011541512.1:p.Asn72Thr
XM_011543210.2:c.215A>C	XP_011541512.1:p.Asn72Thr
XM_017009118.1:c.524A>C	XP_016864607.1:p.Asn175Thr
XM_024454381.1:c.161A>C	XP_024310149.1:p.Asn54Thr
XR_002959845.1:n.814A>C
XR_246533.3:n.814A>C