Canonical Allele Identifier: CA2202662053
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3249725_3249726delinsTG , CM000678.2:g.3249725_3249726delinsTG GRCh38
NC_000016.9:g.3299725_3299726delinsTG , CM000678.1:g.3299725_3299726delinsTG GRCh37
NC_000016.8:g.3239726_3239727delinsTG NCBI36
NG_007871.1:g.11902_11903delinsCA , LRG_190:g.11902_11903delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000219596.6:c.965_966delinsCA MANE Select ENSP00000219596.1:p.Pro322=
ENST00000219596.5:c.965_966delinsCA ENSP00000219596.1:p.Pro322=
ENST00000339854.8:c.425_426delinsCA ENSP00000339639.4:p.Pro142=
ENST00000536379.5:c.332_333delinsCA ENSP00000445079.1:p.Pro111=
ENST00000536980.5:c.332_333delinsCA ENSP00000444178.1:p.Pro111=
ENST00000537682.5:c.965_966delinsCA ENSP00000438611.1:p.Pro322=
ENST00000538326.5:c.965_966delinsCA ENSP00000437486.1:p.Pro322=
ENST00000539145.5:c.278-2480_278-2479delinsCA ENSP00000444471.1:n.278-2480_278-2479delinsCA
ENST00000541159.5:c.332_333delinsCA ENSP00000438711.1:p.Pro111=
ENST00000542898.5:c.1058_1059delinsCA ENSP00000444615.1:p.Pro353=
ENST00000570511.5:c.911-2480_911-2479delinsCA ENSP00000458312.1:n.911-2480_911-2479delinsCA
ENST00000572244.5:c.278-3179_278-3178delinsCA ENSP00000461186.1:n.278-3179_278-3178delinsCA
ENST00000574583.5:c.278-2480_278-2479delinsCA ENSP00000460269.1:n.278-2480_278-2479delinsCA
ENST00000576315.5:c.278-2480_278-2479delinsCA ENSP00000460551.1:n.278-2480_278-2479delinsCA
ENST00000621655.1:c.332_333delinsCA ENSP00000481436.1:p.Pro111=
NM_000243.2:c.965_966delinsCA , LRG_190t1:c.965_966delinsCA NP_000234.1:p.Pro322=
NM_001198536.1:c.332_333delinsCA NP_001185465.1:p.Pro111=
XM_017023236.2:c.965_966delinsCA XP_016878725.1:p.Pro322=
XR_001751903.1:n.1154_1155delinsCA
NM_000243.3:c.965_966delinsCA MANE Select NP_000234.1:p.Pro322=
NM_001198536.2:c.332_333delinsCA NP_001185465.2:p.Pro111=