Canonical Allele Identifier: CA1928689104

Gene: FFAR4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93588378_93588379delinsCA , CM000672.2:g.93588378_93588379delinsCA	GRCh38
NC_000010.10:g.95348135_95348136delinsCA , CM000672.1:g.95348135_95348136delinsCA	GRCh37
NC_000010.9:g.95338125_95338126delinsCA	NCBI36
NG_032670.1:g.26714_26715delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000371481.9:c.*769_*770delinsCA MANE Select	ENSP00000360536.5:n.*769_*770delinsCA
ENST00000371481.8:c.*769_*770delinsCA	ENSP00000360536.4:n.*769_*770delinsCA
ENST00000371483.8:c.*769_*770delinsCA	ENSP00000360538.4:n.*769_*770delinsCA
ENST00000604414.1:c.696+12159_696+12160delinsCA	ENSP00000474477.1:n.696+12159_696+12160de...
NM_001195755.1:c.*769_*770delinsCA	NP_001182684.1:n.*769_*770delinsCA
NM_181745.3:c.*769_*770delinsCA	NP_859529.2:n.*769_*770delinsCA
NM_001195755.2:c.*769_*770delinsCA MANE Select	NP_001182684.1:n.*769_*770delinsCA
NM_181745.4:c.*769_*770delinsCA	NP_859529.2:n.*769_*770delinsCA