Canonical Allele Identifier: CA340132538

Gene: MMACHC

Linked Data

• MyVariant Identifiers: chr1:g.45974032A>T (hg19) ; chr1:g.45508360A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45508360A>T , CM000663.2:g.45508360A>T	GRCh38
NC_000001.10:g.45974032A>T , CM000663.1:g.45974032A>T	GRCh37
NC_000001.9:g.45746619A>T	NCBI36
NG_013378.1:g.13177A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000401061.9:c.425A>T MANE Select	ENSP00000383840.4:p.Asn142Ile
ENST00000401061.8:c.425A>T	ENSP00000383840.4:p.Asn142Ile
ENST00000616135.1:c.254A>T	ENSP00000478859.1:p.Asn85Ile
NM_015506.2:c.425A>T	NP_056321.2:p.Asn142Ile
XM_005270724.3:c.230A>T	XP_005270781.1:p.Asn77Ile
XM_011541204.1:c.254A>T	XP_011539506.1:p.Asn85Ile
NM_001330540.1:c.254A>T	NP_001317469.1:p.Asn85Ile
XM_005270724.5:c.230A>T	XP_005270781.1:p.Asn77Ile
NM_015506.3:c.425A>T MANE Select	NP_056321.2:p.Asn142Ile
NM_001330540.2:c.254A>T	NP_001317469.1:p.Asn85Ile