Canonical Allele Identifier: CA2645390979

Gene: MMACHC

Linked Data

• gnomAD v4: 1-45508645-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45508645G>T , CM000663.2:g.45508645G>T	GRCh38
NC_000001.10:g.45974317G>T , CM000663.1:g.45974317G>T	GRCh37
NC_000001.9:g.45746904G>T	NCBI36
NG_013378.1:g.13462G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.430-151G>T MANE Select	ENSP00000383840.4:n.430-151G>T
ENST00000401061.8:c.430-151G>T	ENSP00000383840.4:n.430-151G>T
ENST00000616135.1:c.259-151G>T	ENSP00000478859.1:n.259-151G>T
NM_015506.2:c.430-151G>T	NP_056321.2:n.430-151G>T
XM_005270724.3:c.235-151G>T	XP_005270781.1:n.235-151G>T
XM_011541204.1:c.259-151G>T	XP_011539506.1:n.259-151G>T
NM_001330540.1:c.259-151G>T	NP_001317469.1:n.259-151G>T
XM_005270724.5:c.235-151G>T	XP_005270781.1:n.235-151G>T
NM_015506.3:c.430-151G>T MANE Select	NP_056321.2:n.430-151G>T
NM_001330540.2:c.259-151G>T	NP_001317469.1:n.259-151G>T