Canonical Allele Identifier: CA389967832

Gene: MTHFD1

Linked Data

• gnomAD v4: 14-64411141-G-A
• MyVariant Identifiers: chr14:g.64877859G>A (hg19) ; chr14:g.64411141G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64411141G>A , CM000676.2:g.64411141G>A	GRCh38
NC_000014.8:g.64877859G>A , CM000676.1:g.64877859G>A	GRCh37
NC_000014.7:g.63947612G>A	NCBI36
NG_012450.1:g.28101G>A
NG_012450.2:g.28101G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555858.2:n.327G>A
ENST00000557539.2:c.-66G>A	ENSP00000476468.2:n.-66G>A
ENST00000697166.1:n.327G>A
ENST00000697167.1:c.178G>A	ENSP00000513155.1:p.Ala60Thr
ENST00000697168.1:c.178G>A	ENSP00000513156.1:p.Ala60Thr
ENST00000697169.1:c.178G>A	ENSP00000513157.1:p.Ala60Thr
ENST00000697170.1:n.327G>A
ENST00000697171.1:c.178G>A	ENSP00000513158.1:p.Ala60Thr
ENST00000697173.1:c.-66G>A	ENSP00000513159.1:n.-66G>A
ENST00000697174.1:c.178G>A	ENSP00000513160.1:p.Ala60Thr
ENST00000697175.1:c.-202G>A	ENSP00000513161.1:n.-202G>A
ENST00000697176.1:c.-66G>A	ENSP00000513162.1:n.-66G>A
ENST00000545908.6:c.178G>A	ENSP00000438588.2:p.Ala60Thr
ENST00000554768.6:c.-66G>A	ENSP00000477501.2:n.-66G>A
ENST00000555709.7:c.178G>A	ENSP00000450560.3:p.Ala60Thr
ENST00000557370.3:c.178G>A	ENSP00000477199.2:p.Ala60Thr
ENST00000650853.1:n.253G>A
ENST00000651537.1:c.178G>A	ENSP00000498511.1:p.Ala60Thr
ENST00000652179.1:c.-66G>A	ENSP00000498649.1:n.-66G>A
ENST00000652337.1:c.178G>A MANE Select	ENSP00000498336.1:p.Ala60Thr
ENST00000216605.12:c.178G>A	ENSP00000216605.8:p.Ala60Thr
ENST00000545908.5:c.346G>A	ENSP00000438588.1:p.Ala116Thr
ENST00000554739.5:c.-66G>A	ENSP00000477359.1:n.-66G>A
ENST00000554768.5:c.-66G>A	ENSP00000477501.1:n.-66G>A
ENST00000555252.5:n.244-1331G>A
ENST00000555709.6:c.346G>A	ENSP00000450560.2:p.Ala116Thr
ENST00000557539.1:c.-66G>A	ENSP00000476468.1:n.-66G>A
NM_005956.3:c.178G>A	NP_005947.3:p.Ala60Thr
NM_001364837.1:c.178G>A	NP_001351766.1:p.Ala60Thr
NM_005956.4:c.178G>A MANE Select	NP_005947.3:p.Ala60Thr