Canonical Allele Identifier: CA346710376

Gene: MCFD2

Linked Data

• MyVariant Identifiers: chr2:g.47132622A>C (hg19) ; chr2:g.46905483A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.46905483A>C , CM000664.2:g.46905483A>C	GRCh38
NC_000002.11:g.47132622A>C , CM000664.1:g.47132622A>C	GRCh37
NC_000002.10:g.46986126A>C	NCBI36
NG_016428.2:g.41373T>G , LRG_566:g.41373T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319466.9:c.421T>G MANE Select	ENSP00000317271.4:p.Phe141Val
ENST00000649435.1:c.*87T>G	ENSP00000498024.1:n.*87T>G
ENST00000319466.8:c.421T>G	ENSP00000317271.4:p.Phe141Val
ENST00000409105.5:c.421T>G	ENSP00000386651.1:p.Phe141Val
ENST00000409147.1:c.265T>G	ENSP00000387082.1:p.Phe89Val
ENST00000409207.5:c.421T>G	ENSP00000386386.1:p.Phe141Val
ENST00000409218.5:c.421T>G	ENSP00000386261.1:p.Phe141Val
ENST00000409800.5:c.265T>G	ENSP00000387202.1:p.Phe89Val
ENST00000409913.5:c.265T>G	ENSP00000386941.1:p.Phe89Val
ENST00000409973.5:c.421T>G	ENSP00000386279.1:p.Phe141Val
ENST00000412438.5:c.421T>G	ENSP00000402717.1:p.Phe141Val
ENST00000444761.6:c.364T>G	ENSP00000394647.2:p.Phe122Val
ENST00000470873.1:n.314T>G
ENST00000493804.1:n.179T>G
NM_001171506.2:c.421T>G , LRG_566t1:c.421T>G	NP_001164977.1:p.Phe141Val
NM_001171507.2:c.421T>G , LRG_566t2:c.421T>G	NP_001164978.1:p.Phe141Val
NM_001171508.2:c.421T>G , LRG_566t3:c.421T>G	NP_001164979.1:p.Phe141Val
NM_001171509.2:c.265T>G	NP_001164980.1:p.Phe89Val
NM_001171510.2:c.265T>G	NP_001164981.1:p.Phe89Val
NM_001171511.2:c.364T>G	NP_001164982.1:p.Phe122Val
NM_139279.5:c.421T>G , LRG_566t4:c.421T>G	NP_644808.1:p.Phe141Val
NM_001171509.3:c.265T>G	NP_001164980.1:p.Phe89Val
NM_001171510.3:c.265T>G	NP_001164981.1:p.Phe89Val
NM_139279.6:c.421T>G MANE Select	NP_644808.1:p.Phe141Val
NM_001171511.3:c.364T>G	NP_001164982.1:p.Phe122Val