Canonical Allele Identifier: CA340133706

Gene: MMACHC

Linked Data

• MyVariant Identifiers: chr1:g.45974658A>T (hg19) ; chr1:g.45508986A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45508986A>T , CM000663.2:g.45508986A>T	GRCh38
NC_000001.10:g.45974658A>T , CM000663.1:g.45974658A>T	GRCh37
NC_000001.9:g.45747245A>T	NCBI36
NG_013378.1:g.13803A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.620A>T MANE Select	ENSP00000383840.4:p.Asp207Val
ENST00000401061.8:c.620A>T	ENSP00000383840.4:p.Asp207Val
ENST00000616135.1:c.449A>T	ENSP00000478859.1:p.Asp150Val
NM_015506.2:c.620A>T	NP_056321.2:p.Asp207Val
XM_005270724.3:c.425A>T	XP_005270781.1:p.Asp142Val
XM_011541204.1:c.449A>T	XP_011539506.1:p.Asp150Val
NM_001330540.1:c.449A>T	NP_001317469.1:p.Asp150Val
XM_005270724.5:c.425A>T	XP_005270781.1:p.Asp142Val
NM_015506.3:c.620A>T MANE Select	NP_056321.2:p.Asp207Val
NM_001330540.2:c.449A>T	NP_001317469.1:p.Asp150Val