Canonical Allele Identifier: CA486711028

Gene: MTHFD1

Linked Data

• MyVariant Identifiers: chr14:g.64882393T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64415675T>A , CM000676.2:g.64415675T>A	GRCh38
NC_000014.8:g.64882393T>A , CM000676.1:g.64882393T>A	GRCh37
NC_000014.7:g.63952146T>A	NCBI36
NG_012450.1:g.32635T>A
NG_012450.2:g.32635T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000555858.2:n.563T>A
ENST00000557539.2:c.171T>A	ENSP00000476468.2:p.Gly57=
ENST00000697166.1:n.563T>A
ENST00000697167.1:c.414T>A	ENSP00000513155.1:p.Gly138=
ENST00000697168.1:c.414T>A	ENSP00000513156.1:p.Gly138=
ENST00000697169.1:c.414T>A	ENSP00000513157.1:p.Gly138=
ENST00000697170.1:n.563T>A
ENST00000697171.1:c.414T>A	ENSP00000513158.1:p.Gly138=
ENST00000697173.1:c.171T>A	ENSP00000513159.1:p.Gly57=
ENST00000697174.1:c.414T>A	ENSP00000513160.1:p.Gly138=
ENST00000697175.1:c.171T>A	ENSP00000513161.1:p.Gly57=
ENST00000697176.1:c.171T>A	ENSP00000513162.1:p.Gly57=
ENST00000545908.6:c.414T>A	ENSP00000438588.2:p.Gly138=
ENST00000554768.6:c.171T>A	ENSP00000477501.2:p.Gly57=
ENST00000555709.7:c.414T>A	ENSP00000450560.3:p.Gly138=
ENST00000557370.3:c.414T>A	ENSP00000477199.2:p.Gly138=
ENST00000650853.1:n.489T>A
ENST00000651537.1:c.414T>A	ENSP00000498511.1:p.Gly138=
ENST00000652179.1:c.171T>A	ENSP00000498649.1:p.Gly57=
ENST00000652337.1:c.414T>A MANE Select	ENSP00000498336.1:p.Gly138=
ENST00000652503.1:n.38T>A
ENST00000216605.12:c.414T>A	ENSP00000216605.8:p.Gly138=
ENST00000545908.5:c.582T>A	ENSP00000438588.1:p.Gly194=
ENST00000555252.5:n.471T>A
ENST00000555709.6:c.582T>A	ENSP00000450560.2:p.Gly194=
ENST00000557539.1:c.171T>A	ENSP00000476468.1:p.Gly57=
NM_005956.3:c.414T>A	NP_005947.3:p.Gly138=
NM_001364837.1:c.414T>A	NP_001351766.1:p.Gly138=
NM_005956.4:c.414T>A MANE Select	NP_005947.3:p.Gly138=