Canonical Allele Identifier: CA493384378
Gene: MEFV HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.3304651A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3254651A>G , CM000678.2:g.3254651A>G GRCh38
NC_000016.9:g.3304651A>G , CM000678.1:g.3304651A>G GRCh37
NC_000016.8:g.3244652A>G NCBI36
NG_007871.1:g.6977T>C , LRG_190:g.6977T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000219596.6:c.417T>C MANE Select ENSP00000219596.1:p.Ala139=
ENST00000219596.5:c.417T>C ENSP00000219596.1:p.Ala139=
ENST00000339854.8:c.277+1660T>C ENSP00000339639.4:n.277+1660T>C
ENST00000536379.5:c.277+1660T>C ENSP00000445079.1:n.277+1660T>C
ENST00000536980.5:c.277+1660T>C ENSP00000444178.1:n.277+1660T>C
ENST00000537682.5:c.417T>C ENSP00000438611.1:p.Ala139=
ENST00000538326.5:c.417T>C ENSP00000437486.1:p.Ala139=
ENST00000539145.5:c.277+1660T>C ENSP00000444471.1:n.277+1660T>C
ENST00000541159.5:c.277+1660T>C ENSP00000438711.1:n.277+1660T>C
ENST00000542898.5:c.417T>C ENSP00000444615.1:p.Ala139=
ENST00000570511.5:c.417T>C ENSP00000458312.1:p.Ala139=
ENST00000572244.5:c.277+1660T>C ENSP00000461186.1:n.277+1660T>C
ENST00000574583.5:c.277+1660T>C ENSP00000460269.1:n.277+1660T>C
ENST00000576315.5:c.277+1660T>C ENSP00000460551.1:n.277+1660T>C
ENST00000621655.1:c.277+1660T>C ENSP00000481436.1:n.277+1660T>C
NM_000243.2:c.417T>C , LRG_190t1:c.417T>C NP_000234.1:p.Ala139=
NM_001198536.1:c.277+1660T>C NP_001185465.1:n.277+1660T>C
XM_017023236.2:c.417T>C XP_016878725.1:p.Ala139=
XR_001751903.1:n.606T>C
NM_000243.3:c.417T>C MANE Select NP_000234.1:p.Ala139=
NM_001198536.2:c.277+1660T>C NP_001185465.2:n.277+1660T>C