Canonical Allele Identifier: CA2035562855

Gene: FAM186A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.50360692T= , CM000674.2:g.50360692T=	GRCh38
NC_000012.11:g.50754475T= , CM000674.1:g.50754475T=	GRCh37
NC_000012.10:g.49040742T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000327337.6:c.583+64A= MANE Select	ENSP00000329995.5:n.583+64A=
ENST00000327337.5:c.583+64A=	ENSP00000329995.5:n.583+64A=
ENST00000543111.5:c.583+64A=	ENSP00000441337.1:n.583+64A=
NM_001145475.1:c.583+64A=	NP_001138947.1:n.583+64A=
XM_006719231.2:c.583+64A=	XP_006719294.1:n.583+64A=
XM_011537890.1:c.583+64A=	XP_011536192.1:n.583+64A=
XM_011537891.1:c.412+2453A=	XP_011536193.1:n.412+2453A=
XM_011537892.1:c.154+64A=	XP_011536194.1:n.154+64A=
NM_001145475.2:c.583+64A=	NP_001138947.1:n.583+64A=
XM_006719231.3:c.583+64A=	XP_006719294.1:n.583+64A=
XM_011537890.2:c.583+64A=	XP_011536192.1:n.583+64A=
NM_001145475.3:c.583+64A= MANE Select	NP_001138947.1:n.583+64A=