Canonical Allele Identifier: CA2610205393

Gene: FFAR4

Linked Data

• gnomAD v4: 10-93588395-C-CTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93588406_93588409dup , CM000672.2:g.93588406_93588409dup	GRCh38
NC_000010.10:g.95348163_95348166dup , CM000672.1:g.95348163_95348166dup	GRCh37
NC_000010.9:g.95338153_95338156dup	NCBI36
NG_032670.1:g.26742_26745dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371481.9:c.*797_*800dup MANE Select	ENSP00000360536.5:n.*797_*800dup
ENST00000371481.8:c.*797_*800dup	ENSP00000360536.4:n.*797_*800dup
ENST00000371483.8:c.*797_*800dup	ENSP00000360538.4:n.*797_*800dup
ENST00000604414.1:c.696+12187_696+12190dup	ENSP00000474477.1:n.696+12187_696+12190dup
NM_001195755.1:c.*797_*800dup	NP_001182684.1:n.*797_*800dup
NM_181745.3:c.*797_*800dup	NP_859529.2:n.*797_*800dup
NM_001195755.2:c.*797_*800dup MANE Select	NP_001182684.1:n.*797_*800dup
NM_181745.4:c.*797_*800dup	NP_859529.2:n.*797_*800dup