Canonical Allele Identifier: CA2202662076
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3249761A= , CM000678.2:g.3249761A= GRCh38
NC_000016.9:g.3299761A= , CM000678.1:g.3299761A= GRCh37
NC_000016.8:g.3239762A= NCBI36
NG_007871.1:g.11867T= , LRG_190:g.11867T=

Transcript Alleles

HGVS Amino-acid change
ENST00000219596.6:c.930T= MANE Select ENSP00000219596.1:p.Ala310=
ENST00000219596.5:c.930T= ENSP00000219596.1:p.Ala310=
ENST00000339854.8:c.390T= ENSP00000339639.4:p.Ala130=
ENST00000536379.5:c.297T= ENSP00000445079.1:p.Ala99=
ENST00000536980.5:c.297T= ENSP00000444178.1:p.Ala99=
ENST00000537682.5:c.930T= ENSP00000438611.1:p.Ala310=
ENST00000538326.5:c.930T= ENSP00000437486.1:p.Ala310=
ENST00000539145.5:c.278-2515T= ENSP00000444471.1:n.278-2515T=
ENST00000541159.5:c.297T= ENSP00000438711.1:p.Ala99=
ENST00000542898.5:c.1023T= ENSP00000444615.1:p.Ala341=
ENST00000570511.5:c.911-2515T= ENSP00000458312.1:n.911-2515T=
ENST00000572244.5:c.278-3214T= ENSP00000461186.1:n.278-3214T=
ENST00000574583.5:c.278-2515T= ENSP00000460269.1:n.278-2515T=
ENST00000576315.5:c.278-2515T= ENSP00000460551.1:n.278-2515T=
ENST00000621655.1:c.297T= ENSP00000481436.1:p.Ala99=
NM_000243.2:c.930T= , LRG_190t1:c.930T= NP_000234.1:p.Ala310=
NM_001198536.1:c.297T= NP_001185465.1:p.Ala99=
XM_017023236.2:c.930T= XP_016878725.1:p.Ala310=
XR_001751903.1:n.1119T=
NM_000243.3:c.930T= MANE Select NP_000234.1:p.Ala310=
NM_001198536.2:c.297T= NP_001185465.2:p.Ala99=