Canonical Allele Identifier: CA2618746716

Gene: FAM186A

Linked Data

• gnomAD v4: 12-50360690-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.50360690_50360691insT , CM000674.2:g.50360690_50360691insT	GRCh38
NC_000012.11:g.50754473_50754474insT , CM000674.1:g.50754473_50754474insT	GRCh37
NC_000012.10:g.49040740_49040741insT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000327337.6:c.583+65_583+66insA MANE Select	ENSP00000329995.5:n.583+65_583+66insA
ENST00000327337.5:c.583+65_583+66insA	ENSP00000329995.5:n.583+65_583+66insA
ENST00000543111.5:c.583+65_583+66insA	ENSP00000441337.1:n.583+65_583+66insA
NM_001145475.1:c.583+65_583+66insA	NP_001138947.1:n.583+65_583+66insA
XM_006719231.2:c.583+65_583+66insA	XP_006719294.1:n.583+65_583+66insA
XM_011537890.1:c.583+65_583+66insA	XP_011536192.1:n.583+65_583+66insA
XM_011537891.1:c.412+2454_412+2455insA	XP_011536193.1:n.412+2454_412+2455insA
XM_011537892.1:c.154+65_154+66insA	XP_011536194.1:n.154+65_154+66insA
NM_001145475.2:c.583+65_583+66insA	NP_001138947.1:n.583+65_583+66insA
XM_006719231.3:c.583+65_583+66insA	XP_006719294.1:n.583+65_583+66insA
XM_011537890.2:c.583+65_583+66insA	XP_011536192.1:n.583+65_583+66insA
NM_001145475.3:c.583+65_583+66insA MANE Select	NP_001138947.1:n.583+65_583+66insA