Canonical Allele Identifier: CA2495553707

Gene: MCFD2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.46905489C= , CM000664.2:g.46905489C=	GRCh38
NC_000002.11:g.47132628C= , CM000664.1:g.47132628C=	GRCh37
NC_000002.10:g.46986132C=	NCBI36
NG_016428.2:g.41367G= , LRG_566:g.41367G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319466.9:c.415G= MANE Select	ENSP00000317271.4:p.Ala139=
ENST00000649435.1:c.*81G=	ENSP00000498024.1:n.*81G=
ENST00000319466.8:c.415G=	ENSP00000317271.4:p.Ala139=
ENST00000409105.5:c.415G=	ENSP00000386651.1:p.Ala139=
ENST00000409147.1:c.259G=	ENSP00000387082.1:p.Ala87=
ENST00000409207.5:c.415G=	ENSP00000386386.1:p.Ala139=
ENST00000409218.5:c.415G=	ENSP00000386261.1:p.Ala139=
ENST00000409800.5:c.259G=	ENSP00000387202.1:p.Ala87=
ENST00000409913.5:c.259G=	ENSP00000386941.1:p.Ala87=
ENST00000409973.5:c.415G=	ENSP00000386279.1:p.Ala139=
ENST00000412438.5:c.415G=	ENSP00000402717.1:p.Ala139=
ENST00000444761.6:c.358G=	ENSP00000394647.2:p.Ala120=
ENST00000470873.1:n.308G=
ENST00000493804.1:n.173G=
NM_001171506.2:c.415G= , LRG_566t1:c.415G=	NP_001164977.1:p.Ala139=
NM_001171507.2:c.415G= , LRG_566t2:c.415G=	NP_001164978.1:p.Ala139=
NM_001171508.2:c.415G= , LRG_566t3:c.415G=	NP_001164979.1:p.Ala139=
NM_001171509.2:c.259G=	NP_001164980.1:p.Ala87=
NM_001171510.2:c.259G=	NP_001164981.1:p.Ala87=
NM_001171511.2:c.358G=	NP_001164982.1:p.Ala120=
NM_139279.5:c.415G= , LRG_566t4:c.415G=	NP_644808.1:p.Ala139=
NM_001171509.3:c.259G=	NP_001164980.1:p.Ala87=
NM_001171510.3:c.259G=	NP_001164981.1:p.Ala87=
NM_139279.6:c.415G= MANE Select	NP_644808.1:p.Ala139=
NM_001171511.3:c.358G=	NP_001164982.1:p.Ala120=