Canonical Allele Identifier: CA1153807122

Gene: MTHFR

Linked Data

• dbSNP Id: rs1644393783

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11801897_11801898insGGGGCCC , CM000663.2:g.11801897_11801898insGGGGCCC	GRCh38
NC_000001.10:g.11861954_11861955insGGGGCCC , CM000663.1:g.11861954_11861955insGGGGCCC	GRCh37
NC_000001.9:g.11784541_11784542insGGGGCCC	NCBI36
NG_008766.1:g.748_749insGGGGCCC
NG_013351.1:g.9208_9209insGCCCCGG , LRG_726:g.9208_9209insGCCCCGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000376486.3:c.237-497_237-496insGCCCCGG	ENSP00000365669.3:n.237-497_237-496insGCC...
ENST00000376585.6:c.360-497_360-496insGCCCCGG	ENSP00000365770.1:n.360-497_360-496insGCC...
ENST00000376590.9:c.237-497_237-496insGCCCCGG MANE Select	ENSP00000365775.3:n.237-497_237-496insGCC...
ENST00000376592.6:c.237-497_237-496insGCCCCGG	ENSP00000365777.1:n.237-497_237-496insGCC...
ENST00000423400.7:c.357-497_357-496insGCCCCGG	ENSP00000398908.3:n.357-497_357-496insGCC...
ENST00000431243.6:n.1018-480_1018-479insGCCCCGG
ENST00000641407.1:c.237-497_237-496insGCCCCGG	ENSP00000493098.1:n.237-497_237-496insGCC...
ENST00000641437.1:n.369-497_369-496insGCCCCGG
ENST00000641446.1:c.237-497_237-496insGCCCCGG	ENSP00000493262.1:n.237-497_237-496insGCC...
ENST00000641721.1:n.294-497_294-496insGCCCCGG
ENST00000641747.1:c.236+985_236+986insGCCCCGG	ENSP00000493116.1:n.236+985_236+986insGCC...
ENST00000641759.1:n.372-497_372-496insGCCCCGG
ENST00000641805.1:n.520-497_520-496insGCCCCGG
ENST00000641909.1:n.647-497_647-496insGCCCCGG
ENST00000642002.1:n.466-480_466-479insGCCCCGG
ENST00000376583.7:c.360-497_360-496insGCCCCGG	ENSP00000365767.3:n.360-497_360-496insGCC...
ENST00000376585.5:c.360-497_360-496insGCCCCGG	ENSP00000365770.1:n.360-497_360-496insGCC...
ENST00000376590.7:c.237-497_237-496insGCCCCGG	ENSP00000365775.3:n.237-497_237-496insGCC...
ENST00000376592.5:c.237-497_237-496insGCCCCGG	ENSP00000365777.1:n.237-497_237-496insGCC...
ENST00000418034.1:c.237-497_237-496insGCCCCGG	ENSP00000405082.1:n.237-497_237-496insGCC...
NM_005957.4:c.237-497_237-496insGCCCCGG , LRG_726t1:c.237-497_237-496insGCCCCGG	NP_005948.3:n.237-497_237-496insGCCCCGG
XM_005263458.2:c.360-497_360-496insGCCCCGG	XP_005263515.1:n.360-497_360-496insGCCCCG...
XM_005263460.3:c.237-497_237-496insGCCCCGG	XP_005263517.1:n.237-497_237-496insGCCCCG...
XM_005263461.3:c.237-497_237-496insGCCCCGG	XP_005263518.1:n.237-497_237-496insGCCCCG...
XM_005263462.3:c.237-497_237-496insGCCCCGG	XP_005263519.1:n.237-497_237-496insGCCCCG...
XM_005263463.2:c.-27-480_-27-479insGCCCCGG	XP_005263520.1:n.-27-480_-27-479insGCCCCG...
XM_011541495.1:c.357-497_357-496insGCCCCGG	XP_011539797.1:n.357-497_357-496insGCCCCG...
XM_011541496.1:c.360-497_360-496insGCCCCGG	XP_011539798.1:n.360-497_360-496insGCCCCG...
NM_001330358.1:c.360-497_360-496insGCCCCGG	NP_001317287.1:n.360-497_360-496insGCCCCG...
XM_005263460.5:c.237-497_237-496insGCCCCGG	XP_005263517.1:n.237-497_237-496insGCCCCG...
XM_005263462.4:c.237-497_237-496insGCCCCGG	XP_005263519.1:n.237-497_237-496insGCCCCG...
XM_005263463.4:c.-27-480_-27-479insGCCCCGG	XP_005263520.1:n.-27-480_-27-479insGCCCCG...
XM_011541495.3:c.357-497_357-496insGCCCCGG	XP_011539797.1:n.357-497_357-496insGCCCCG...
XM_011541496.3:c.360-497_360-496insGCCCCGG	XP_011539798.1:n.360-497_360-496insGCCCCG...
XM_017001328.2:c.360-497_360-496insGCCCCGG	XP_016856817.1:n.360-497_360-496insGCCCCG...
XM_024447198.1:c.-27-480_-27-479insGCCCCGG	XP_024302966.1:n.-27-480_-27-479insGCCCCG...
XR_002956640.1:n.1104-497_1104-496insGCCCCGG
NM_005957.5:c.237-497_237-496insGCCCCGG MANE Select	NP_005948.3:n.237-497_237-496insGCCCCGG
NM_001330358.2:c.360-497_360-496insGCCCCGG	NP_001317287.1:n.360-497_360-496insGCCCCG...