Canonical Allele Identifier: CA394458400

Gene: MEFV

Linked Data

• gnomAD v4: 16-3244526-T-G
• MyVariant Identifiers: chr16:g.3294526T>G (hg19) ; chr16:g.3244526T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244526T>G , CM000678.2:g.3244526T>G	GRCh38
NC_000016.9:g.3294526T>G , CM000678.1:g.3294526T>G	GRCh37
NC_000016.8:g.3234527T>G	NCBI36
NG_007871.1:g.17102A>C , LRG_190:g.17102A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.794A>C
ENST00000219596.6:c.1673A>C MANE Select	ENSP00000219596.1:p.Gln558Pro
ENST00000219596.5:c.1673A>C	ENSP00000219596.1:p.Gln558Pro
ENST00000339854.8:c.1133A>C	ENSP00000339639.4:p.Gln378Pro
ENST00000536379.5:c.1040A>C	ENSP00000445079.1:p.Gln347Pro
ENST00000536980.5:c.1040A>C	ENSP00000444178.1:p.Gln347Pro
ENST00000537682.5:c.1673A>C	ENSP00000438611.1:p.Gln558Pro
ENST00000538326.5:c.*298A>C	ENSP00000437486.1:n.*298A>C
ENST00000539145.5:c.594A>C	ENSP00000444471.1:n.594A>C
ENST00000541159.5:c.1040A>C	ENSP00000438711.1:p.Gln347Pro
ENST00000542898.5:c.1766A>C	ENSP00000444615.1:p.Gln589Pro
ENST00000570511.5:c.1165-634A>C	ENSP00000458312.1:n.1165-634A>C
ENST00000572244.5:c.363A>C	ENSP00000461186.1:n.363A>C
ENST00000574583.5:c.532-634A>C	ENSP00000460269.1:n.532-634A>C
ENST00000576315.5:c.532-240A>C	ENSP00000460551.1:n.532-240A>C
ENST00000621655.1:c.1040A>C	ENSP00000481436.1:p.Gln347Pro
NM_000243.2:c.1673A>C , LRG_190t1:c.1673A>C	NP_000234.1:p.Gln558Pro
NM_001198536.1:c.1040A>C	NP_001185465.1:p.Gln347Pro
XM_017023236.2:c.1670A>C	XP_016878725.1:p.Gln557Pro
XR_001751903.1:n.1862A>C
NM_000243.3:c.1673A>C MANE Select	NP_000234.1:p.Gln558Pro
NM_001198536.2:c.1040A>C	NP_001185465.2:p.Gln347Pro