Canonical Allele Identifier: CA1928689117
Gene: FFAR4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93588395C= , CM000672.2:g.93588395C= GRCh38
NC_000010.10:g.95348152C= , CM000672.1:g.95348152C= GRCh37
NC_000010.9:g.95338142C= NCBI36
NG_032670.1:g.26731C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371481.9:c.*786C= MANE Select ENSP00000360536.5:n.*786C=
ENST00000371481.8:c.*786C= ENSP00000360536.4:n.*786C=
ENST00000371483.8:c.*786C= ENSP00000360538.4:n.*786C=
ENST00000604414.1:c.696+12176C= ENSP00000474477.1:n.696+12176C=
NM_001195755.1:c.*786C= NP_001182684.1:n.*786C=
NM_181745.3:c.*786C= NP_859529.2:n.*786C=
NM_001195755.2:c.*786C= MANE Select NP_001182684.1:n.*786C=
NM_181745.4:c.*786C= NP_859529.2:n.*786C=
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