Canonical Allele Identifier: CA340133712

Gene: MMACHC

Linked Data

• MyVariant Identifiers: chr1:g.45974659T>G (hg19) ; chr1:g.45508987T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45508987T>G , CM000663.2:g.45508987T>G	GRCh38
NC_000001.10:g.45974659T>G , CM000663.1:g.45974659T>G	GRCh37
NC_000001.9:g.45747246T>G	NCBI36
NG_013378.1:g.13804T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000401061.9:c.621T>G MANE Select	ENSP00000383840.4:p.Asp207Glu
ENST00000401061.8:c.621T>G	ENSP00000383840.4:p.Asp207Glu
ENST00000616135.1:c.450T>G	ENSP00000478859.1:p.Asp150Glu
NM_015506.2:c.621T>G	NP_056321.2:p.Asp207Glu
XM_005270724.3:c.426T>G	XP_005270781.1:p.Asp142Glu
XM_011541204.1:c.450T>G	XP_011539506.1:p.Asp150Glu
NM_001330540.1:c.450T>G	NP_001317469.1:p.Asp150Glu
XM_005270724.5:c.426T>G	XP_005270781.1:p.Asp142Glu
NM_015506.3:c.621T>G MANE Select	NP_056321.2:p.Asp207Glu
NM_001330540.2:c.450T>G	NP_001317469.1:p.Asp150Glu