Canonical Allele Identifier: CA886104426

Gene: MTHFR

Linked Data

• dbSNP Id: rs786204005
• gnomAD v3: 1-11803156-A-ATG
• gnomAD v4: 1-11803156-A-ATG
• MyVariant Identifiers: chr1:g.11863213_11863214insTG (hg19) ; chr1:g.11803156_11803157insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11803156_11803157insTG , CM000663.2:g.11803156_11803157insTG	GRCh38
NC_000001.10:g.11863213_11863214insTG , CM000663.1:g.11863213_11863214insTG	GRCh37
NC_000001.9:g.11785800_11785801insTG	NCBI36
NG_008766.1:g.2007_2008insTG
NG_013351.1:g.7947_7948insCA , LRG_726:g.7947_7948insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.-10-31_-10-30insCA	ENSP00000365669.3:n.-10-31_-10-30insCA
ENST00000376585.6:c.111-28_111-27insCA	ENSP00000365770.1:n.111-28_111-27insCA
ENST00000376590.9:c.-13-28_-13-27insCA MANE Select	ENSP00000365775.3:n.-13-28_-13-27insCA
ENST00000376592.6:c.-41_-40insCA	ENSP00000365777.1:n.-41_-40insCA
ENST00000423400.7:c.111-31_111-30insCA	ENSP00000398908.3:n.111-31_111-30insCA
ENST00000431243.6:n.769-28_769-27insCA
ENST00000641407.1:c.-41_-40insCA	ENSP00000493098.1:n.-41_-40insCA
ENST00000641437.1:n.120-28_120-27insCA
ENST00000641446.1:c.-13-28_-13-27insCA	ENSP00000493262.1:n.-13-28_-13-27insCA
ENST00000641721.1:n.45-28_45-27insCA
ENST00000641747.1:c.-13-28_-13-27insCA	ENSP00000493116.1:n.-13-28_-13-27insCA
ENST00000641759.1:n.123-28_123-27insCA
ENST00000641805.1:n.274-31_274-30insCA
ENST00000641909.1:n.370_371insCA
ENST00000642002.1:n.217-28_217-27insCA
ENST00000376486.2:c.-13-28_-13-27insCA	ENSP00000365669.2:n.-13-28_-13-27insCA
ENST00000376583.7:c.111-28_111-27insCA	ENSP00000365767.3:n.111-28_111-27insCA
ENST00000376585.5:c.111-28_111-27insCA	ENSP00000365770.1:n.111-28_111-27insCA
ENST00000376590.7:c.-13-28_-13-27insCA	ENSP00000365775.3:n.-13-28_-13-27insCA
ENST00000376592.5:c.-41_-40insCA	ENSP00000365777.1:n.-41_-40insCA
ENST00000413656.5:c.-13-28_-13-27insCA	ENSP00000408307.1:n.-13-28_-13-27insCA
ENST00000418034.1:c.-13-28_-13-27insCA	ENSP00000405082.1:n.-13-28_-13-27insCA
ENST00000423400.5:c.29_30insCA	ENSP00000398908.1:p.Asp11MetfsTer16
ENST00000431243.5:c.-13-28_-13-27insCA	ENSP00000400460.1:n.-13-28_-13-27insCA
NM_005957.4:c.-13-28_-13-27insCA , LRG_726t1:c.-13-28_-13-27insCA	NP_005948.3:n.-13-28_-13-27insCA
XM_005263458.2:c.111-28_111-27insCA	XP_005263515.1:n.111-28_111-27insCA
XM_005263460.3:c.-13-28_-13-27insCA	XP_005263517.1:n.-13-28_-13-27insCA
XM_005263461.3:c.-10-31_-10-30insCA	XP_005263518.1:n.-10-31_-10-30insCA
XM_005263462.3:c.-10-31_-10-30insCA	XP_005263519.1:n.-10-31_-10-30insCA
XM_005263463.2:c.-276-28_-276-27insCA	XP_005263520.1:n.-276-28_-276-27insCA
XM_011541495.1:c.111-31_111-30insCA	XP_011539797.1:n.111-31_111-30insCA
XM_011541496.1:c.111-28_111-27insCA	XP_011539798.1:n.111-28_111-27insCA
NM_001330358.1:c.111-28_111-27insCA	NP_001317287.1:n.111-28_111-27insCA
XM_005263460.5:c.-13-28_-13-27insCA	XP_005263517.1:n.-13-28_-13-27insCA
XM_005263462.4:c.-10-31_-10-30insCA	XP_005263519.1:n.-10-31_-10-30insCA
XM_005263463.4:c.-276-28_-276-27insCA	XP_005263520.1:n.-276-28_-276-27insCA
XM_011541495.3:c.111-31_111-30insCA	XP_011539797.1:n.111-31_111-30insCA
XM_011541496.3:c.111-28_111-27insCA	XP_011539798.1:n.111-28_111-27insCA
XM_017001328.2:c.111-28_111-27insCA	XP_016856817.1:n.111-28_111-27insCA
XM_024447198.1:c.-276-28_-276-27insCA	XP_024302966.1:n.-276-28_-276-27insCA
XR_002956640.1:n.858-31_858-30insCA
NM_005957.5:c.-13-28_-13-27insCA MANE Select	NP_005948.3:n.-13-28_-13-27insCA
NM_001330358.2:c.111-28_111-27insCA	NP_001317287.1:n.111-28_111-27insCA