Canonical Allele Identifier: CA2610208254

Gene: FFAR4

Linked Data

• gnomAD v4: 10-93588266-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93588266G>T , CM000672.2:g.93588266G>T	GRCh38
NC_000010.10:g.95348023G>T , CM000672.1:g.95348023G>T	GRCh37
NC_000010.9:g.95338013G>T	NCBI36
NG_032670.1:g.26602G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371481.9:c.*657G>T MANE Select	ENSP00000360536.5:n.*657G>T
ENST00000371481.8:c.*657G>T	ENSP00000360536.4:n.*657G>T
ENST00000371483.8:c.*657G>T	ENSP00000360538.4:n.*657G>T
ENST00000604414.1:c.696+12047G>T	ENSP00000474477.1:n.696+12047G>T
NM_001195755.1:c.*657G>T	NP_001182684.1:n.*657G>T
NM_181745.3:c.*657G>T	NP_859529.2:n.*657G>T
NM_001195755.2:c.*657G>T MANE Select	NP_001182684.1:n.*657G>T
NM_181745.4:c.*657G>T	NP_859529.2:n.*657G>T