Canonical Allele Identifier: CA2618746707

Gene: FAM186A

Linked Data

• gnomAD v4: 12-50360686-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.50360686_50360687insC , CM000674.2:g.50360686_50360687insC	GRCh38
NC_000012.11:g.50754469_50754470insC , CM000674.1:g.50754469_50754470insC	GRCh37
NC_000012.10:g.49040736_49040737insC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000327337.6:c.583+69_583+70insG MANE Select	ENSP00000329995.5:n.583+69_583+70insG
ENST00000327337.5:c.583+69_583+70insG	ENSP00000329995.5:n.583+69_583+70insG
ENST00000543111.5:c.583+69_583+70insG	ENSP00000441337.1:n.583+69_583+70insG
NM_001145475.1:c.583+69_583+70insG	NP_001138947.1:n.583+69_583+70insG
XM_006719231.2:c.583+69_583+70insG	XP_006719294.1:n.583+69_583+70insG
XM_011537890.1:c.583+69_583+70insG	XP_011536192.1:n.583+69_583+70insG
XM_011537891.1:c.412+2458_412+2459insG	XP_011536193.1:n.412+2458_412+2459insG
XM_011537892.1:c.154+69_154+70insG	XP_011536194.1:n.154+69_154+70insG
NM_001145475.2:c.583+69_583+70insG	NP_001138947.1:n.583+69_583+70insG
XM_006719231.3:c.583+69_583+70insG	XP_006719294.1:n.583+69_583+70insG
XM_011537890.2:c.583+69_583+70insG	XP_011536192.1:n.583+69_583+70insG
NM_001145475.3:c.583+69_583+70insG MANE Select	NP_001138947.1:n.583+69_583+70insG