Canonical Allele Identifier: CA338422179
Gene: MTHFR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11801176T>A , CM000663.2:g.11801176T>A GRCh38
NC_000001.10:g.11861233T>A , CM000663.1:g.11861233T>A GRCh37
NC_000001.9:g.11783820T>A NCBI36
NG_008766.1:g.27T>A
NG_013351.1:g.9928A>T , LRG_726:g.9928A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376486.3:c.460A>T ENSP00000365669.3:p.Met154Leu
ENST00000376585.6:c.583A>T ENSP00000365770.1:p.Met195Leu
ENST00000376590.9:c.460A>T MANE Select ENSP00000365775.3:p.Met154Leu
ENST00000376592.6:c.460A>T ENSP00000365777.1:p.Met154Leu
ENST00000423400.7:c.580A>T ENSP00000398908.3:p.Met194Leu
ENST00000641407.1:c.460A>T ENSP00000493098.1:p.Met154Leu
ENST00000641437.1:n.592A>T
ENST00000641446.1:c.460A>T ENSP00000493262.1:p.Met154Leu
ENST00000641721.1:n.517A>T
ENST00000641747.1:c.237-854A>T ENSP00000493116.1:n.237-854A>T
ENST00000641759.1:n.595A>T
ENST00000641805.1:n.743A>T
ENST00000641909.1:n.870A>T
ENST00000376583.7:c.583A>T ENSP00000365767.3:p.Met195Leu
ENST00000376585.5:c.583A>T ENSP00000365770.1:p.Met195Leu
ENST00000376590.7:c.460A>T ENSP00000365775.3:p.Met154Leu
ENST00000376592.5:c.460A>T ENSP00000365777.1:p.Met154Leu
NM_005957.4:c.460A>T , LRG_726t1:c.460A>T NP_005948.3:p.Met154Leu
XM_005263458.2:c.583A>T XP_005263515.1:p.Met195Leu
XM_005263460.3:c.460A>T XP_005263517.1:p.Met154Leu
XM_005263461.3:c.460A>T XP_005263518.1:p.Met154Leu
XM_005263462.3:c.460A>T XP_005263519.1:p.Met154Leu
XM_005263463.2:c.214A>T XP_005263520.1:p.Met72Leu
XM_011541495.1:c.580A>T XP_011539797.1:p.Met194Leu
XM_011541496.1:c.583A>T XP_011539798.1:p.Met195Leu
NM_001330358.1:c.583A>T NP_001317287.1:p.Met195Leu
XM_005263460.5:c.460A>T XP_005263517.1:p.Met154Leu
XM_005263462.4:c.460A>T XP_005263519.1:p.Met154Leu
XM_005263463.4:c.214A>T XP_005263520.1:p.Met72Leu
XM_011541495.3:c.580A>T XP_011539797.1:p.Met194Leu
XM_011541496.3:c.583A>T XP_011539798.1:p.Met195Leu
XM_017001328.2:c.583A>T XP_016856817.1:p.Met195Leu
XM_024447198.1:c.214A>T XP_024302966.1:p.Met72Leu
XR_002956640.1:n.1327A>T
NM_005957.5:c.460A>T MANE Select NP_005948.3:p.Met154Leu
NM_001330358.2:c.583A>T NP_001317287.1:p.Met195Leu