Canonical Allele Identifier: CA2574214289

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11794963_11794966del , CM000663.2:g.11794963_11794966del	GRCh38
NC_000001.10:g.11855020_11855023del , CM000663.1:g.11855020_11855023del	GRCh37
NC_000001.9:g.11777607_11777610del	NCBI36
NG_013351.1:g.16138_16141del , LRG_726:g.16138_16141del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.1155-103_1155-100del	ENSP00000365770.1:n.1155-103_1155-100del
ENST00000376590.9:c.1032-103_1032-100del MANE Select	ENSP00000365775.3:n.1032-103_1032-100del
ENST00000376592.6:c.1032-103_1032-100del	ENSP00000365777.1:n.1032-103_1032-100del
ENST00000423400.7:c.1152-103_1152-100del	ENSP00000398908.3:n.1152-103_1152-100del
ENST00000641407.1:c.1032-103_1032-100del	ENSP00000493098.1:n.1032-103_1032-100del
ENST00000641446.1:c.1032-103_1032-100del	ENSP00000493262.1:n.1032-103_1032-100del
ENST00000641747.1:c.*544-103_*544-100del	ENSP00000493116.1:n.*544-103_*544-100del
ENST00000641759.1:n.1298_1301del
ENST00000641805.1:n.1446_1449del
ENST00000641820.1:c.297-103_297-100del	ENSP00000492937.1:n.297-103_297-100del
ENST00000376583.7:c.1155-103_1155-100del	ENSP00000365767.3:n.1155-103_1155-100del
ENST00000376585.5:c.1155-103_1155-100del	ENSP00000365770.1:n.1155-103_1155-100del
ENST00000376590.7:c.1032-103_1032-100del	ENSP00000365775.3:n.1032-103_1032-100del
ENST00000376592.5:c.1032-103_1032-100del	ENSP00000365777.1:n.1032-103_1032-100del
NM_005957.4:c.1032-103_1032-100del , LRG_726t1:c.1032-103_1032-100del	NP_005948.3:n.1032-103_1032-100del
XM_005263458.2:c.1155-103_1155-100del	XP_005263515.1:n.1155-103_1155-100del
XM_005263460.3:c.1032-103_1032-100del	XP_005263517.1:n.1032-103_1032-100del
XM_005263461.3:c.1032-103_1032-100del	XP_005263518.1:n.1032-103_1032-100del
XM_005263462.3:c.1032-103_1032-100del	XP_005263519.1:n.1032-103_1032-100del
XM_005263463.2:c.786-103_786-100del	XP_005263520.1:n.786-103_786-100del
XM_011541495.1:c.1152-103_1152-100del	XP_011539797.1:n.1152-103_1152-100del
XM_011541496.1:c.1155-103_1155-100del	XP_011539798.1:n.1155-103_1155-100del
NM_001330358.1:c.1155-103_1155-100del	NP_001317287.1:n.1155-103_1155-100del
XM_005263460.5:c.1032-103_1032-100del	XP_005263517.1:n.1032-103_1032-100del
XM_005263462.4:c.1032-103_1032-100del	XP_005263519.1:n.1032-103_1032-100del
XM_005263463.4:c.786-103_786-100del	XP_005263520.1:n.786-103_786-100del
XM_011541495.3:c.1152-103_1152-100del	XP_011539797.1:n.1152-103_1152-100del
XM_011541496.3:c.1155-103_1155-100del	XP_011539798.1:n.1155-103_1155-100del
XM_017001328.2:c.1155-103_1155-100del	XP_016856817.1:n.1155-103_1155-100del
XM_024447198.1:c.786-103_786-100del	XP_024302966.1:n.786-103_786-100del
XR_002956640.1:n.2030_2033del
NM_005957.5:c.1032-103_1032-100del MANE Select	NP_005948.3:n.1032-103_1032-100del
NM_001330358.2:c.1155-103_1155-100del	NP_001317287.1:n.1155-103_1155-100del