Canonical Allele Identifier: CA2202658355

Gene: MEFV

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3242872A= , CM000678.2:g.3242872A=	GRCh38
NC_000016.9:g.3292872A= , CM000678.1:g.3292872A=	GRCh37
NC_000016.8:g.3232873A=	NCBI36
NG_007871.1:g.18756T= , LRG_190:g.18756T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1736T=
ENST00000219596.6:c.*269T= MANE Select	ENSP00000219596.1:n.*269T=
ENST00000219596.5:c.*269T=	ENSP00000219596.1:n.*269T=
ENST00000339854.8:c.*269T=	ENSP00000339639.4:n.*269T=
ENST00000536980.5:c.*891T=	ENSP00000444178.1:n.*891T=
ENST00000537682.5:c.*891T=	ENSP00000438611.1:n.*891T=
ENST00000538326.5:c.*1240T=	ENSP00000437486.1:n.*1240T=
ENST00000542898.5:c.*891T=	ENSP00000444615.1:n.*891T=
NM_000243.2:c.*269T= , LRG_190t1:c.*269T=	NP_000234.1:n.*269T=
NM_001198536.1:c.*819T=	NP_001185465.1:n.*819T=
NM_000243.3:c.*269T= MANE Select	NP_000234.1:n.*269T=
NM_001198536.2:c.*819T=	NP_001185465.2:n.*819T=