Canonical Allele Identifier: CA2495553729

Gene: MCFD2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.46905541T= , CM000664.2:g.46905541T=	GRCh38
NC_000002.11:g.47132680T= , CM000664.1:g.47132680T=	GRCh37
NC_000002.10:g.46986184T=	NCBI36
NG_016428.2:g.41315A= , LRG_566:g.41315A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319466.9:c.363A= MANE Select	ENSP00000317271.4:p.Ile121=
ENST00000649435.1:c.*29A=	ENSP00000498024.1:n.*29A=
ENST00000319466.8:c.363A=	ENSP00000317271.4:p.Ile121=
ENST00000409105.5:c.363A=	ENSP00000386651.1:p.Ile121=
ENST00000409147.1:c.207A=	ENSP00000387082.1:p.Ile69=
ENST00000409207.5:c.363A=	ENSP00000386386.1:p.Ile121=
ENST00000409218.5:c.363A=	ENSP00000386261.1:p.Ile121=
ENST00000409800.5:c.207A=	ENSP00000387202.1:p.Ile69=
ENST00000409913.5:c.207A=	ENSP00000386941.1:p.Ile69=
ENST00000409973.5:c.363A=	ENSP00000386279.1:p.Ile121=
ENST00000412438.5:c.363A=	ENSP00000402717.1:p.Ile121=
ENST00000444761.6:c.306A=	ENSP00000394647.2:p.Ile102=
ENST00000470873.1:n.256A=
ENST00000493804.1:n.121A=
NM_001171506.2:c.363A= , LRG_566t1:c.363A=	NP_001164977.1:p.Ile121=
NM_001171507.2:c.363A= , LRG_566t2:c.363A=	NP_001164978.1:p.Ile121=
NM_001171508.2:c.363A= , LRG_566t3:c.363A=	NP_001164979.1:p.Ile121=
NM_001171509.2:c.207A=	NP_001164980.1:p.Ile69=
NM_001171510.2:c.207A=	NP_001164981.1:p.Ile69=
NM_001171511.2:c.306A=	NP_001164982.1:p.Ile102=
NM_139279.5:c.363A= , LRG_566t4:c.363A=	NP_644808.1:p.Ile121=
NM_001171509.3:c.207A=	NP_001164980.1:p.Ile69=
NM_001171510.3:c.207A=	NP_001164981.1:p.Ile69=
NM_139279.6:c.363A= MANE Select	NP_644808.1:p.Ile121=
NM_001171511.3:c.306A=	NP_001164982.1:p.Ile102=