Canonical Allele Identifier: CA7225921
Gene: MTHFD1 HGNC NCBI

Linked Data

dbSNP Id: rs765289796

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64415593C>T , CM000676.2:g.64415593C>T GRCh38
NC_000014.8:g.64882311C>T , CM000676.1:g.64882311C>T GRCh37
NC_000014.7:g.63952064C>T NCBI36
NG_012450.1:g.32553C>T
NG_012450.2:g.32553C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000555858.2:n.527-46C>T
ENST00000557539.2:c.135-46C>T ENSP00000476468.2:n.135-46C>T
ENST00000697166.1:n.527-46C>T
ENST00000697167.1:c.378-46C>T ENSP00000513155.1:n.378-46C>T
ENST00000697168.1:c.378-46C>T ENSP00000513156.1:n.378-46C>T
ENST00000697169.1:c.378-46C>T ENSP00000513157.1:n.378-46C>T
ENST00000697170.1:n.527-46C>T
ENST00000697171.1:c.378-46C>T ENSP00000513158.1:n.378-46C>T
ENST00000697173.1:c.135-46C>T ENSP00000513159.1:n.135-46C>T
ENST00000697174.1:c.378-46C>T ENSP00000513160.1:n.378-46C>T
ENST00000697175.1:c.135-46C>T ENSP00000513161.1:n.135-46C>T
ENST00000697176.1:c.135-46C>T ENSP00000513162.1:n.135-46C>T
ENST00000545908.6:c.378-46C>T ENSP00000438588.2:n.378-46C>T
ENST00000554768.6:c.135-46C>T ENSP00000477501.2:n.135-46C>T
ENST00000555709.7:c.378-46C>T ENSP00000450560.3:n.378-46C>T
ENST00000557370.3:c.378-46C>T ENSP00000477199.2:n.378-46C>T
ENST00000650853.1:n.453-46C>T
ENST00000651537.1:c.378-46C>T ENSP00000498511.1:n.378-46C>T
ENST00000652179.1:c.135-46C>T ENSP00000498649.1:n.135-46C>T
ENST00000652337.1:c.378-46C>T MANE Select ENSP00000498336.1:n.378-46C>T
ENST00000216605.12:c.378-46C>T ENSP00000216605.8:n.378-46C>T
ENST00000545908.5:c.546-46C>T ENSP00000438588.1:n.546-46C>T
ENST00000555252.5:n.435-46C>T
ENST00000555709.6:c.546-46C>T ENSP00000450560.2:n.546-46C>T
ENST00000557539.1:c.135-46C>T ENSP00000476468.1:n.135-46C>T
NM_005956.3:c.378-46C>T NP_005947.3:n.378-46C>T
NM_001364837.1:c.378-46C>T NP_001351766.1:n.378-46C>T
NM_005956.4:c.378-46C>T MANE Select NP_005947.3:n.378-46C>T