Canonical Allele Identifier: CA2575889926
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3256592C>G , CM000678.2:g.3256592C>G GRCh38
NC_000016.9:g.3306592C>G , CM000678.1:g.3306592C>G GRCh37
NC_000016.8:g.3246593C>G NCBI36
NG_007871.1:g.5036G>C , LRG_190:g.5036G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000219596.6:c.-5G>C MANE Select ENSP00000219596.1:n.-5G>C
ENST00000219596.5:c.-5G>C ENSP00000219596.1:n.-5G>C
ENST00000339854.8:c.-5G>C ENSP00000339639.4:n.-5G>C
ENST00000536980.5:c.-5G>C ENSP00000444178.1:n.-5G>C
ENST00000537682.5:c.-5G>C ENSP00000438611.1:n.-5G>C
ENST00000538326.5:c.-5G>C ENSP00000437486.1:n.-5G>C
ENST00000542898.5:c.-5G>C ENSP00000444615.1:n.-5G>C
NM_000243.2:c.-5G>C , LRG_190t1:c.-5G>C NP_000234.1:n.-5G>C
NM_001198536.1:c.-5G>C NP_001185465.1:n.-5G>C
XM_017023236.2:c.-5G>C XP_016878725.1:n.-5G>C
XR_001751903.1:n.185G>C
NM_000243.3:c.-5G>C MANE Select NP_000234.1:n.-5G>C
NM_001198536.2:c.-5G>C NP_001185465.2:n.-5G>C