Canonical Allele Identifier: CA2473783313
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508136C= , CM000663.2:g.45508136C= GRCh38
NC_000001.10:g.45973808C= , CM000663.1:g.45973808C= GRCh37
NC_000001.9:g.45746395C= NCBI36
NG_013378.1:g.12953C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.9:c.277-76C= MANE Select ENSP00000383840.4:n.277-76C=
ENST00000401061.8:c.277-76C= ENSP00000383840.4:n.277-76C=
ENST00000616135.1:c.106-76C= ENSP00000478859.1:n.106-76C=
NM_015506.2:c.277-76C= NP_056321.2:n.277-76C=
XM_005270724.3:c.82-76C= XP_005270781.1:n.82-76C=
XM_011541204.1:c.106-76C= XP_011539506.1:n.106-76C=
NM_001330540.1:c.106-76C= NP_001317469.1:n.106-76C=
XM_005270724.5:c.82-76C= XP_005270781.1:n.82-76C=
NM_015506.3:c.277-76C= MANE Select NP_056321.2:n.277-76C=
NM_001330540.2:c.106-76C= NP_001317469.1:n.106-76C=