Canonical Allele Identifier: CA340128687

Gene: MMACHC

Linked Data

• MyVariant Identifiers: chr1:g.45966066T>A (hg19) ; chr1:g.45500394T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45500394T>A , CM000663.2:g.45500394T>A	GRCh38
NC_000001.10:g.45966066T>A , CM000663.1:g.45966066T>A	GRCh37
NC_000001.9:g.45738653T>A	NCBI36
NG_013378.1:g.5211T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.62T>A MANE Select	ENSP00000383840.4:p.Phe21Tyr
ENST00000401061.8:c.62T>A	ENSP00000383840.4:p.Phe21Tyr
ENST00000616135.1:c.-110T>A	ENSP00000478859.1:n.-110T>A
NM_015506.2:c.62T>A	NP_056321.2:p.Phe21Tyr
XM_005270724.3:c.62T>A	XP_005270781.1:p.Phe21Tyr
XM_011541204.1:c.-161T>A	XP_011539506.1:n.-161T>A
NM_001330540.1:c.-161T>A	NP_001317469.1:n.-161T>A
XM_005270724.5:c.62T>A	XP_005270781.1:p.Phe21Tyr
NM_015506.3:c.62T>A MANE Select	NP_056321.2:p.Phe21Tyr
NM_001330540.2:c.-161T>A	NP_001317469.1:n.-161T>A