Canonical Allele Identifier: CA2618746706

Gene: FAM186A

Linked Data

• gnomAD v4: 12-50360685-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.50360685_50360686insG , CM000674.2:g.50360685_50360686insG	GRCh38
NC_000012.11:g.50754468_50754469insG , CM000674.1:g.50754468_50754469insG	GRCh37
NC_000012.10:g.49040735_49040736insG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000327337.6:c.583+70_583+71insC MANE Select	ENSP00000329995.5:n.583+70_583+71insC
ENST00000327337.5:c.583+70_583+71insC	ENSP00000329995.5:n.583+70_583+71insC
ENST00000543111.5:c.583+70_583+71insC	ENSP00000441337.1:n.583+70_583+71insC
NM_001145475.1:c.583+70_583+71insC	NP_001138947.1:n.583+70_583+71insC
XM_006719231.2:c.583+70_583+71insC	XP_006719294.1:n.583+70_583+71insC
XM_011537890.1:c.583+70_583+71insC	XP_011536192.1:n.583+70_583+71insC
XM_011537891.1:c.412+2459_412+2460insC	XP_011536193.1:n.412+2459_412+2460insC
XM_011537892.1:c.154+70_154+71insC	XP_011536194.1:n.154+70_154+71insC
NM_001145475.2:c.583+70_583+71insC	NP_001138947.1:n.583+70_583+71insC
XM_006719231.3:c.583+70_583+71insC	XP_006719294.1:n.583+70_583+71insC
XM_011537890.2:c.583+70_583+71insC	XP_011536192.1:n.583+70_583+71insC
NM_001145475.3:c.583+70_583+71insC MANE Select	NP_001138947.1:n.583+70_583+71insC