Canonical Allele Identifier: CA340131348
Community Standard Title: NM_015506.3(MMACHC):c.82-1G>A
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45507355G>A , CM000663.2:g.45507355G>A GRCh38
NC_000001.10:g.45973027G>A , CM000663.1:g.45973027G>A GRCh37
NC_000001.9:g.45745614G>A NCBI36
NG_013378.1:g.12172G>A

Transcript Alleles

HGVS Amino-acid Change
NM_015506.3:c.82-1G>A MANE Select NP_056321.2:n.82-1G>A
ENST00000401061.9:c.82-1G>A MANE Select ENSP00000383840.4:n.82-1G>A
NM_001330540.1:c.-91G>A NP_001317469.1:n.-91G>A
NM_001330540.2:c.-91G>A NP_001317469.1:n.-91G>A
NM_015506.2:c.82-1G>A NP_056321.2:n.82-1G>A
ENST00000401061.8:c.82-1G>A ENSP00000383840.4:n.82-1G>A
ENST00000616135.1:c.-90-1G>A ENSP00000478859.1:n.-90-1G>A
XM_005270724.3:c.82-857G>A XP_005270781.1:n.82-857G>A
XM_005270724.5:c.82-857G>A XP_005270781.1:n.82-857G>A
XM_011541204.1:c.-91G>A XP_011539506.1:n.-91G>A