Canonical Allele Identifier: CA340133948

Gene: MMACHC

Linked Data

• MyVariant Identifiers: chr1:g.45974711A>G (hg19) ; chr1:g.45509039A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45509039A>G , CM000663.2:g.45509039A>G	GRCh38
NC_000001.10:g.45974711A>G , CM000663.1:g.45974711A>G	GRCh37
NC_000001.9:g.45747298A>G	NCBI36
NG_013378.1:g.13856A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000401061.9:c.673A>G MANE Select	ENSP00000383840.4:p.Thr225Ala
ENST00000401061.8:c.673A>G	ENSP00000383840.4:p.Thr225Ala
ENST00000616135.1:c.502A>G	ENSP00000478859.1:p.Thr168Ala
NM_015506.2:c.673A>G	NP_056321.2:p.Thr225Ala
XM_005270724.3:c.478A>G	XP_005270781.1:p.Thr160Ala
XM_011541204.1:c.502A>G	XP_011539506.1:p.Thr168Ala
NM_001330540.1:c.502A>G	NP_001317469.1:p.Thr168Ala
XM_005270724.5:c.478A>G	XP_005270781.1:p.Thr160Ala
NM_015506.3:c.673A>G MANE Select	NP_056321.2:p.Thr225Ala
NM_001330540.2:c.502A>G	NP_001317469.1:p.Thr168Ala