Canonical Allele Identifier: CA389967561
Gene: MTHFD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64411120A>C , CM000676.2:g.64411120A>C GRCh38
NC_000014.8:g.64877838A>C , CM000676.1:g.64877838A>C GRCh37
NC_000014.7:g.63947591A>C NCBI36
NG_012450.1:g.28080A>C
NG_012450.2:g.28080A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000555858.2:n.306A>C
ENST00000557539.2:c.-87A>C ENSP00000476468.2:n.-87A>C
ENST00000697166.1:n.306A>C
ENST00000697167.1:c.157A>C ENSP00000513155.1:p.Ile53Leu
ENST00000697168.1:c.157A>C ENSP00000513156.1:p.Ile53Leu
ENST00000697169.1:c.157A>C ENSP00000513157.1:p.Ile53Leu
ENST00000697170.1:n.306A>C
ENST00000697171.1:c.157A>C ENSP00000513158.1:p.Ile53Leu
ENST00000697173.1:c.-87A>C ENSP00000513159.1:n.-87A>C
ENST00000697174.1:c.157A>C ENSP00000513160.1:p.Ile53Leu
ENST00000697175.1:c.-223A>C ENSP00000513161.1:n.-223A>C
ENST00000697176.1:c.-87A>C ENSP00000513162.1:n.-87A>C
ENST00000545908.6:c.157A>C ENSP00000438588.2:p.Ile53Leu
ENST00000554768.6:c.-87A>C ENSP00000477501.2:n.-87A>C
ENST00000555709.7:c.157A>C ENSP00000450560.3:p.Ile53Leu
ENST00000557370.3:c.157A>C ENSP00000477199.2:p.Ile53Leu
ENST00000650853.1:n.232A>C
ENST00000651537.1:c.157A>C ENSP00000498511.1:p.Ile53Leu
ENST00000652179.1:c.-87A>C ENSP00000498649.1:n.-87A>C
ENST00000652337.1:c.157A>C MANE Select ENSP00000498336.1:p.Ile53Leu
ENST00000216605.12:c.157A>C ENSP00000216605.8:p.Ile53Leu
ENST00000545908.5:c.325A>C ENSP00000438588.1:p.Ile109Leu
ENST00000554739.5:c.-87A>C ENSP00000477359.1:n.-87A>C
ENST00000554768.5:c.-87A>C ENSP00000477501.1:n.-87A>C
ENST00000555252.5:n.244-1352A>C
ENST00000555709.6:c.325A>C ENSP00000450560.2:p.Ile109Leu
ENST00000557539.1:c.-87A>C ENSP00000476468.1:n.-87A>C
NM_005956.3:c.157A>C NP_005947.3:p.Ile53Leu
NM_001364837.1:c.157A>C NP_001351766.1:p.Ile53Leu
NM_005956.4:c.157A>C MANE Select NP_005947.3:p.Ile53Leu