Canonical Allele Identifier: CA2202665968
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3256522_3256523delinsCT , CM000678.2:g.3256522_3256523delinsCT GRCh38
NC_000016.9:g.3306522_3306523delinsCT , CM000678.1:g.3306522_3306523delinsCT GRCh37
NC_000016.8:g.3246523_3246524delinsCT NCBI36
NG_007871.1:g.5105_5106delinsAG , LRG_190:g.5105_5106delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000219596.6:c.65_66delinsAG MANE Select ENSP00000219596.1:p.Glu22=
ENST00000219596.5:c.65_66delinsAG ENSP00000219596.1:p.Glu22=
ENST00000339854.8:c.65_66delinsAG ENSP00000339639.4:p.Glu22=
ENST00000536379.5:c.65_66delinsAG ENSP00000445079.1:p.Glu22=
ENST00000536980.5:c.65_66delinsAG ENSP00000444178.1:p.Glu22=
ENST00000537682.5:c.65_66delinsAG ENSP00000438611.1:p.Glu22=
ENST00000538326.5:c.65_66delinsAG ENSP00000437486.1:p.Glu22=
ENST00000539145.5:c.65_66delinsAG ENSP00000444471.1:p.Glu22=
ENST00000541159.5:c.65_66delinsAG ENSP00000438711.1:p.Glu22=
ENST00000542898.5:c.65_66delinsAG ENSP00000444615.1:p.Glu22=
ENST00000570511.5:c.65_66delinsAG ENSP00000458312.1:p.Glu22=
ENST00000572244.5:c.65_66delinsAG ENSP00000461186.1:p.Glu22=
ENST00000574583.5:c.65_66delinsAG ENSP00000460269.1:p.Glu22=
ENST00000576315.5:c.65_66delinsAG ENSP00000460551.1:p.Glu22=
ENST00000621655.1:c.65_66delinsAG ENSP00000481436.1:p.Glu22=
NM_000243.2:c.65_66delinsAG , LRG_190t1:c.65_66delinsAG NP_000234.1:p.Glu22=
NM_001198536.1:c.65_66delinsAG NP_001185465.1:p.Glu22=
XM_017023236.2:c.65_66delinsAG XP_016878725.1:p.Glu22=
XR_001751903.1:n.254_255delinsAG
NM_000243.3:c.65_66delinsAG MANE Select NP_000234.1:p.Glu22=
NM_001198536.2:c.65_66delinsAG NP_001185465.2:p.Glu22=