Canonical Allele Identifier: CA2645390886

Gene: MMACHC

Linked Data

• gnomAD v4: 1-45508367-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45508367G>A , CM000663.2:g.45508367G>A	GRCh38
NC_000001.10:g.45974039G>A , CM000663.1:g.45974039G>A	GRCh37
NC_000001.9:g.45746626G>A	NCBI36
NG_013378.1:g.13184G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000401061.9:c.429+3G>A MANE Select	ENSP00000383840.4:n.429+3G>A
ENST00000401061.8:c.429+3G>A	ENSP00000383840.4:n.429+3G>A
ENST00000616135.1:c.258+3G>A	ENSP00000478859.1:n.258+3G>A
NM_015506.2:c.429+3G>A	NP_056321.2:n.429+3G>A
XM_005270724.3:c.234+3G>A	XP_005270781.1:n.234+3G>A
XM_011541204.1:c.258+3G>A	XP_011539506.1:n.258+3G>A
NM_001330540.1:c.258+3G>A	NP_001317469.1:n.258+3G>A
XM_005270724.5:c.234+3G>A	XP_005270781.1:n.234+3G>A
NM_015506.3:c.429+3G>A MANE Select	NP_056321.2:n.429+3G>A
NM_001330540.2:c.258+3G>A	NP_001317469.1:n.258+3G>A