Canonical Allele Identifier: CA389967849

Gene: MTHFD1

Linked Data

• gnomAD v4: 14-64411142-C-T
• MyVariant Identifiers: chr14:g.64877860C>T (hg19) ; chr14:g.64411142C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64411142C>T , CM000676.2:g.64411142C>T	GRCh38
NC_000014.8:g.64877860C>T , CM000676.1:g.64877860C>T	GRCh37
NC_000014.7:g.63947613C>T	NCBI36
NG_012450.1:g.28102C>T
NG_012450.2:g.28102C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555858.2:n.328C>T
ENST00000557539.2:c.-65C>T	ENSP00000476468.2:n.-65C>T
ENST00000697166.1:n.328C>T
ENST00000697167.1:c.179C>T	ENSP00000513155.1:p.Ala60Val
ENST00000697168.1:c.179C>T	ENSP00000513156.1:p.Ala60Val
ENST00000697169.1:c.179C>T	ENSP00000513157.1:p.Ala60Val
ENST00000697170.1:n.328C>T
ENST00000697171.1:c.179C>T	ENSP00000513158.1:p.Ala60Val
ENST00000697173.1:c.-65C>T	ENSP00000513159.1:n.-65C>T
ENST00000697174.1:c.179C>T	ENSP00000513160.1:p.Ala60Val
ENST00000697175.1:c.-201C>T	ENSP00000513161.1:n.-201C>T
ENST00000697176.1:c.-65C>T	ENSP00000513162.1:n.-65C>T
ENST00000545908.6:c.179C>T	ENSP00000438588.2:p.Ala60Val
ENST00000554768.6:c.-65C>T	ENSP00000477501.2:n.-65C>T
ENST00000555709.7:c.179C>T	ENSP00000450560.3:p.Ala60Val
ENST00000557370.3:c.179C>T	ENSP00000477199.2:p.Ala60Val
ENST00000650853.1:n.254C>T
ENST00000651537.1:c.179C>T	ENSP00000498511.1:p.Ala60Val
ENST00000652179.1:c.-65C>T	ENSP00000498649.1:n.-65C>T
ENST00000652337.1:c.179C>T MANE Select	ENSP00000498336.1:p.Ala60Val
ENST00000216605.12:c.179C>T	ENSP00000216605.8:p.Ala60Val
ENST00000545908.5:c.347C>T	ENSP00000438588.1:p.Ala116Val
ENST00000554739.5:c.-65C>T	ENSP00000477359.1:n.-65C>T
ENST00000554768.5:c.-65C>T	ENSP00000477501.1:n.-65C>T
ENST00000555252.5:n.244-1330C>T
ENST00000555709.6:c.347C>T	ENSP00000450560.2:p.Ala116Val
ENST00000557539.1:c.-65C>T	ENSP00000476468.1:n.-65C>T
NM_005956.3:c.179C>T	NP_005947.3:p.Ala60Val
NM_001364837.1:c.179C>T	NP_001351766.1:p.Ala60Val
NM_005956.4:c.179C>T MANE Select	NP_005947.3:p.Ala60Val