Canonical Allele Identifier: CA346710348
Gene: MCFD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46905476T>G , CM000664.2:g.46905476T>G GRCh38
NC_000002.11:g.47132615T>G , CM000664.1:g.47132615T>G GRCh37
NC_000002.10:g.46986119T>G NCBI36
NG_016428.2:g.41380A>C , LRG_566:g.41380A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000319466.9:c.428A>C MANE Select ENSP00000317271.4:p.Lys143Thr
ENST00000649435.1:c.*94A>C ENSP00000498024.1:n.*94A>C
ENST00000319466.8:c.428A>C ENSP00000317271.4:p.Lys143Thr
ENST00000409105.5:c.428A>C ENSP00000386651.1:p.Lys143Thr
ENST00000409147.1:c.272A>C ENSP00000387082.1:p.Lys91Thr
ENST00000409207.5:c.428A>C ENSP00000386386.1:p.Lys143Thr
ENST00000409218.5:c.428A>C ENSP00000386261.1:p.Lys143Thr
ENST00000409800.5:c.272A>C ENSP00000387202.1:p.Lys91Thr
ENST00000409913.5:c.272A>C ENSP00000386941.1:p.Lys91Thr
ENST00000409973.5:c.428A>C ENSP00000386279.1:p.Lys143Thr
ENST00000412438.5:c.428A>C ENSP00000402717.1:p.Lys143Thr
ENST00000444761.6:c.371A>C ENSP00000394647.2:p.Lys124Thr
ENST00000470873.1:n.321A>C
ENST00000493804.1:n.186A>C
NM_001171506.2:c.428A>C , LRG_566t1:c.428A>C NP_001164977.1:p.Lys143Thr
NM_001171507.2:c.428A>C , LRG_566t2:c.428A>C NP_001164978.1:p.Lys143Thr
NM_001171508.2:c.428A>C , LRG_566t3:c.428A>C NP_001164979.1:p.Lys143Thr
NM_001171509.2:c.272A>C NP_001164980.1:p.Lys91Thr
NM_001171510.2:c.272A>C NP_001164981.1:p.Lys91Thr
NM_001171511.2:c.371A>C NP_001164982.1:p.Lys124Thr
NM_139279.5:c.428A>C , LRG_566t4:c.428A>C NP_644808.1:p.Lys143Thr
NM_001171509.3:c.272A>C NP_001164980.1:p.Lys91Thr
NM_001171510.3:c.272A>C NP_001164981.1:p.Lys91Thr
NM_139279.6:c.428A>C MANE Select NP_644808.1:p.Lys143Thr
NM_001171511.3:c.371A>C NP_001164982.1:p.Lys124Thr