Canonical Allele Identifier: CA2542787297

Gene: MMACHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45508637T>C , CM000663.2:g.45508637T>C	GRCh38
NC_000001.10:g.45974309T>C , CM000663.1:g.45974309T>C	GRCh37
NC_000001.9:g.45746896T>C	NCBI36
NG_013378.1:g.13454T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.430-159T>C MANE Select	ENSP00000383840.4:n.430-159T>C
ENST00000401061.8:c.430-159T>C	ENSP00000383840.4:n.430-159T>C
ENST00000616135.1:c.259-159T>C	ENSP00000478859.1:n.259-159T>C
NM_015506.2:c.430-159T>C	NP_056321.2:n.430-159T>C
XM_005270724.3:c.235-159T>C	XP_005270781.1:n.235-159T>C
XM_011541204.1:c.259-159T>C	XP_011539506.1:n.259-159T>C
NM_001330540.1:c.259-159T>C	NP_001317469.1:n.259-159T>C
XM_005270724.5:c.235-159T>C	XP_005270781.1:n.235-159T>C
NM_015506.3:c.430-159T>C MANE Select	NP_056321.2:n.430-159T>C
NM_001330540.2:c.259-159T>C	NP_001317469.1:n.259-159T>C