Canonical Allele Identifier: CA1928689100
Gene: FFAR4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93588357A= , CM000672.2:g.93588357A= GRCh38
NC_000010.10:g.95348114A= , CM000672.1:g.95348114A= GRCh37
NC_000010.9:g.95338104A= NCBI36
NG_032670.1:g.26693A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371481.9:c.*748A= MANE Select ENSP00000360536.5:n.*748A=
ENST00000371481.8:c.*748A= ENSP00000360536.4:n.*748A=
ENST00000371483.8:c.*748A= ENSP00000360538.4:n.*748A=
ENST00000604414.1:c.696+12138A= ENSP00000474477.1:n.696+12138A=
NM_001195755.1:c.*748A= NP_001182684.1:n.*748A=
NM_181745.3:c.*748A= NP_859529.2:n.*748A=
NM_001195755.2:c.*748A= MANE Select NP_001182684.1:n.*748A=
NM_181745.4:c.*748A= NP_859529.2:n.*748A=
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