Canonical Allele Identifier: CA1153807175

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11801921_11801924delinsCTCA , CM000663.2:g.11801921_11801924delinsCTCA	GRCh38
NC_000001.10:g.11861978_11861981delinsCTCA , CM000663.1:g.11861978_11861981delinsCTCA	GRCh37
NC_000001.9:g.11784565_11784568delinsCTCA	NCBI36
NG_008766.1:g.772_775delinsCTCA
NG_013351.1:g.9180_9183delinsTGAG , LRG_726:g.9180_9183delinsTGAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000376486.3:c.237-525_237-522delinsTGAG	ENSP00000365669.3:n.237-525_237-522delins...
ENST00000376585.6:c.360-525_360-522delinsTGAG	ENSP00000365770.1:n.360-525_360-522delins...
ENST00000376590.9:c.237-525_237-522delinsTGAG MANE Select	ENSP00000365775.3:n.237-525_237-522delins...
ENST00000376592.6:c.237-525_237-522delinsTGAG	ENSP00000365777.1:n.237-525_237-522delins...
ENST00000423400.7:c.357-525_357-522delinsTGAG	ENSP00000398908.3:n.357-525_357-522delins...
ENST00000431243.6:n.1018-508_1018-505delinsTGAG
ENST00000641407.1:c.237-525_237-522delinsTGAG	ENSP00000493098.1:n.237-525_237-522delins...
ENST00000641437.1:n.369-525_369-522delinsTGAG
ENST00000641446.1:c.237-525_237-522delinsTGAG	ENSP00000493262.1:n.237-525_237-522delins...
ENST00000641721.1:n.294-525_294-522delinsTGAG
ENST00000641747.1:c.236+957_236+960delinsTGAG	ENSP00000493116.1:n.236+957_236+960delins...
ENST00000641759.1:n.372-525_372-522delinsTGAG
ENST00000641805.1:n.520-525_520-522delinsTGAG
ENST00000641909.1:n.647-525_647-522delinsTGAG
ENST00000642002.1:n.466-508_466-505delinsTGAG
ENST00000376583.7:c.360-525_360-522delinsTGAG	ENSP00000365767.3:n.360-525_360-522delins...
ENST00000376585.5:c.360-525_360-522delinsTGAG	ENSP00000365770.1:n.360-525_360-522delins...
ENST00000376590.7:c.237-525_237-522delinsTGAG	ENSP00000365775.3:n.237-525_237-522delins...
ENST00000376592.5:c.237-525_237-522delinsTGAG	ENSP00000365777.1:n.237-525_237-522delins...
ENST00000418034.1:c.237-525_237-522delinsTGAG	ENSP00000405082.1:n.237-525_237-522delins...
NM_005957.4:c.237-525_237-522delinsTGAG , LRG_726t1:c.237-525_237-522delinsTGAG	NP_005948.3:n.237-525_237-522delinsTGAG
XM_005263458.2:c.360-525_360-522delinsTGAG	XP_005263515.1:n.360-525_360-522delinsTGA...
XM_005263460.3:c.237-525_237-522delinsTGAG	XP_005263517.1:n.237-525_237-522delinsTGA...
XM_005263461.3:c.237-525_237-522delinsTGAG	XP_005263518.1:n.237-525_237-522delinsTGA...
XM_005263462.3:c.237-525_237-522delinsTGAG	XP_005263519.1:n.237-525_237-522delinsTGA...
XM_005263463.2:c.-27-508_-27-505delinsTGAG	XP_005263520.1:n.-27-508_-27-505delinsTGA...
XM_011541495.1:c.357-525_357-522delinsTGAG	XP_011539797.1:n.357-525_357-522delinsTGA...
XM_011541496.1:c.360-525_360-522delinsTGAG	XP_011539798.1:n.360-525_360-522delinsTGA...
NM_001330358.1:c.360-525_360-522delinsTGAG	NP_001317287.1:n.360-525_360-522delinsTGA...
XM_005263460.5:c.237-525_237-522delinsTGAG	XP_005263517.1:n.237-525_237-522delinsTGA...
XM_005263462.4:c.237-525_237-522delinsTGAG	XP_005263519.1:n.237-525_237-522delinsTGA...
XM_005263463.4:c.-27-508_-27-505delinsTGAG	XP_005263520.1:n.-27-508_-27-505delinsTGA...
XM_011541495.3:c.357-525_357-522delinsTGAG	XP_011539797.1:n.357-525_357-522delinsTGA...
XM_011541496.3:c.360-525_360-522delinsTGAG	XP_011539798.1:n.360-525_360-522delinsTGA...
XM_017001328.2:c.360-525_360-522delinsTGAG	XP_016856817.1:n.360-525_360-522delinsTGA...
XM_024447198.1:c.-27-508_-27-505delinsTGAG	XP_024302966.1:n.-27-508_-27-505delinsTGA...
XR_002956640.1:n.1104-525_1104-522delinsTGAG
NM_005957.5:c.237-525_237-522delinsTGAG MANE Select	NP_005948.3:n.237-525_237-522delinsTGAG
NM_001330358.2:c.360-525_360-522delinsTGAG	NP_001317287.1:n.360-525_360-522delinsTGA...