Canonical Allele Identifier: CA340132051

Gene: MMACHC

Linked Data

• gnomAD v4: 1-45507537-G-C
• MyVariant Identifiers: chr1:g.45973209G>C (hg19) ; chr1:g.45507537G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45507537G>C , CM000663.2:g.45507537G>C	GRCh38
NC_000001.10:g.45973209G>C , CM000663.1:g.45973209G>C	GRCh37
NC_000001.9:g.45745796G>C	NCBI36
NG_013378.1:g.12354G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.263G>C MANE Select	ENSP00000383840.4:p.Gly88Ala
ENST00000401061.8:c.263G>C	ENSP00000383840.4:p.Gly88Ala
ENST00000616135.1:c.92G>C	ENSP00000478859.1:p.Gly31Ala
NM_015506.2:c.263G>C	NP_056321.2:p.Gly88Ala
XM_005270724.3:c.82-675G>C	XP_005270781.1:n.82-675G>C
XM_011541204.1:c.92G>C	XP_011539506.1:p.Gly31Ala
NM_001330540.1:c.92G>C	NP_001317469.1:p.Gly31Ala
XM_005270724.5:c.82-675G>C	XP_005270781.1:n.82-675G>C
NM_015506.3:c.263G>C MANE Select	NP_056321.2:p.Gly88Ala
NM_001330540.2:c.92G>C	NP_001317469.1:p.Gly31Ala