Canonical Allele Identifier: CA1928689099
Gene: FFAR4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93588353G= , CM000672.2:g.93588353G= GRCh38
NC_000010.10:g.95348110G= , CM000672.1:g.95348110G= GRCh37
NC_000010.9:g.95338100G= NCBI36
NG_032670.1:g.26689G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371481.9:c.*744G= MANE Select ENSP00000360536.5:n.*744G=
ENST00000371481.8:c.*744G= ENSP00000360536.4:n.*744G=
ENST00000371483.8:c.*744G= ENSP00000360538.4:n.*744G=
ENST00000604414.1:c.696+12134G= ENSP00000474477.1:n.696+12134G=
NM_001195755.1:c.*744G= NP_001182684.1:n.*744G=
NM_181745.3:c.*744G= NP_859529.2:n.*744G=
NM_001195755.2:c.*744G= MANE Select NP_001182684.1:n.*744G=
NM_181745.4:c.*744G= NP_859529.2:n.*744G=
Search 100 bp 5'
Search 100 bp 3'