Canonical Allele Identifier: CA2618746715

Gene: FAM186A

Linked Data

• gnomAD v4: 12-50360690-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.50360691_50360692del , CM000674.2:g.50360691_50360692del	GRCh38
NC_000012.11:g.50754474_50754475del , CM000674.1:g.50754474_50754475del	GRCh37
NC_000012.10:g.49040741_49040742del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000327337.6:c.583+64_583+65del MANE Select	ENSP00000329995.5:n.583+64_583+65del
ENST00000327337.5:c.583+64_583+65del	ENSP00000329995.5:n.583+64_583+65del
ENST00000543111.5:c.583+64_583+65del	ENSP00000441337.1:n.583+64_583+65del
NM_001145475.1:c.583+64_583+65del	NP_001138947.1:n.583+64_583+65del
XM_006719231.2:c.583+64_583+65del	XP_006719294.1:n.583+64_583+65del
XM_011537890.1:c.583+64_583+65del	XP_011536192.1:n.583+64_583+65del
XM_011537891.1:c.412+2453_412+2454del	XP_011536193.1:n.412+2453_412+2454del
XM_011537892.1:c.154+64_154+65del	XP_011536194.1:n.154+64_154+65del
NM_001145475.2:c.583+64_583+65del	NP_001138947.1:n.583+64_583+65del
XM_006719231.3:c.583+64_583+65del	XP_006719294.1:n.583+64_583+65del
XM_011537890.2:c.583+64_583+65del	XP_011536192.1:n.583+64_583+65del
NM_001145475.3:c.583+64_583+65del MANE Select	NP_001138947.1:n.583+64_583+65del