Canonical Allele Identifier: CA1947028451

Gene: IFITM3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.320772A= , CM000673.2:g.320772A=	GRCh38
NC_000011.9:g.320772A= , CM000673.1:g.320772A=	GRCh37
NC_000011.8:g.310772A=	NCBI36
NG_032755.1:g.5143T=

Transcript Alleles

HGVS	Amino-acid Change
NM_021034.3:c.42T= MANE Select	NP_066362.2:p.Ser14=
ENST00000399808.5:c.42T= MANE Select	ENSP00000382707.4:p.Ser14=
NM_021034.2:c.42T=	NP_066362.2:p.Ser14=
NR_049759.1:n.143T=
NR_049759.2:n.89T=
ENST00000399808.4:c.42T=	ENSP00000382707.4:p.Ser14=
ENST00000526811.4:c.-22T=	ENSP00000432108.1:n.-22T=
ENST00000531688.2:c.42T=	ENSP00000473645.2:p.Ser14=
ENST00000602735.2:c.-22T=	ENSP00000473544.1:n.-22T=
ENST00000679382.1:c.42T=	ENSP00000505839.1:p.Ser14=
ENST00000679433.1:c.-22T=	ENSP00000506209.1:n.-22T=
ENST00000679441.1:c.-22T=	ENSP00000506018.1:n.-22T=
ENST00000679792.1:c.-22T=	ENSP00000505901.1:n.-22T=
ENST00000680023.1:c.-22T=	ENSP00000506536.1:n.-22T=
ENST00000680209.1:c.42T=	ENSP00000505330.1:p.Ser14=
ENST00000680622.1:c.-22T=	ENSP00000505128.1:n.-22T=
ENST00000680720.1:c.-22T=	ENSP00000505213.1:n.-22T=
ENST00000680932.1:n.70T=
ENST00000681184.1:c.-22T=	ENSP00000505002.1:n.-22T=
ENST00000681198.1:c.42T=	ENSP00000506488.1:p.Ser14=
ENST00000681304.1:c.42T=	ENSP00000506507.1:p.Ser14=
ENST00000681748.1:c.-22T=	ENSP00000505936.1:n.-22T=
ENST00000681840.1:c.42T=	ENSP00000505867.1:p.Ser14=