Canonical Allele Identifier: CA2631354504
Gene: MEFV HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3254366_3254369dup , CM000678.2:g.3254366_3254369dup GRCh38
NC_000016.9:g.3304366_3304369dup , CM000678.1:g.3304366_3304369dup GRCh37
NC_000016.8:g.3244367_3244370dup NCBI36
NG_007871.1:g.7259_7262dup , LRG_190:g.7259_7262dup

Transcript Alleles

HGVS Amino-acid change
ENST00000219596.6:c.699_702dup MANE Select ENSP00000219596.1:p.Ser235AlafsTer8
ENST00000219596.5:c.699_702dup ENSP00000219596.1:p.Ser235AlafsTer8
ENST00000339854.8:c.277+1942_277+1945dup ENSP00000339639.4:n.277+1942_277+1945dup
ENST00000536379.5:c.277+1942_277+1945dup ENSP00000445079.1:n.277+1942_277+1945dup
ENST00000536980.5:c.277+1942_277+1945dup ENSP00000444178.1:n.277+1942_277+1945dup
ENST00000537682.5:c.699_702dup ENSP00000438611.1:p.Ser235AlafsTer8
ENST00000538326.5:c.699_702dup ENSP00000437486.1:p.Ser235AlafsTer8
ENST00000539145.5:c.277+1942_277+1945dup ENSP00000444471.1:n.277+1942_277+1945dup
ENST00000541159.5:c.277+1942_277+1945dup ENSP00000438711.1:n.277+1942_277+1945dup
ENST00000542898.5:c.699_702dup ENSP00000444615.1:p.Ser235AlafsTer8
ENST00000570511.5:c.699_702dup ENSP00000458312.1:p.Ser235AlafsTer8
ENST00000572244.5:c.277+1942_277+1945dup ENSP00000461186.1:n.277+1942_277+1945dup
ENST00000574583.5:c.277+1942_277+1945dup ENSP00000460269.1:n.277+1942_277+1945dup
ENST00000576315.5:c.277+1942_277+1945dup ENSP00000460551.1:n.277+1942_277+1945dup
ENST00000621655.1:c.277+1942_277+1945dup ENSP00000481436.1:n.277+1942_277+1945dup
NM_000243.2:c.699_702dup , LRG_190t1:c.699_702dup NP_000234.1:p.Ser235AlafsTer8
NM_001198536.1:c.277+1942_277+1945dup NP_001185465.1:n.277+1942_277+1945dup
XM_017023236.2:c.699_702dup XP_016878725.1:p.Ser235AlafsTer8
XR_001751903.1:n.888_891dup
NM_000243.3:c.699_702dup MANE Select NP_000234.1:p.Ser235AlafsTer8
NM_001198536.2:c.277+1942_277+1945dup NP_001185465.2:n.277+1942_277+1945dup