Canonical Allele Identifier: CA2610205383
Gene: FFAR4 HGNC NCBI

Linked Data

gnomAD v4: 10-93588380-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93588380G>T , CM000672.2:g.93588380G>T GRCh38
NC_000010.10:g.95348137G>T , CM000672.1:g.95348137G>T GRCh37
NC_000010.9:g.95338127G>T NCBI36
NG_032670.1:g.26716G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371481.9:c.*771G>T MANE Select ENSP00000360536.5:n.*771G>T
ENST00000371481.8:c.*771G>T ENSP00000360536.4:n.*771G>T
ENST00000371483.8:c.*771G>T ENSP00000360538.4:n.*771G>T
ENST00000604414.1:c.696+12161G>T ENSP00000474477.1:n.696+12161G>T
NM_001195755.1:c.*771G>T NP_001182684.1:n.*771G>T
NM_181745.3:c.*771G>T NP_859529.2:n.*771G>T
NM_001195755.2:c.*771G>T MANE Select NP_001182684.1:n.*771G>T
NM_181745.4:c.*771G>T NP_859529.2:n.*771G>T
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