Canonical Allele Identifier: CA2696092612

Gene: MMACHC

Linked Data

• dbSNP Id: rs2149323706

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45508582del , CM000663.2:g.45508582del	GRCh38
NC_000001.10:g.45974254del , CM000663.1:g.45974254del	GRCh37
NC_000001.9:g.45746841del	NCBI36
NG_013378.1:g.13399del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.430-214del MANE Select	ENSP00000383840.4:n.430-214del
ENST00000401061.8:c.430-214del	ENSP00000383840.4:n.430-214del
ENST00000616135.1:c.259-214del	ENSP00000478859.1:n.259-214del
NM_015506.2:c.430-214del	NP_056321.2:n.430-214del
XM_005270724.3:c.235-214del	XP_005270781.1:n.235-214del
XM_011541204.1:c.259-214del	XP_011539506.1:n.259-214del
NM_001330540.1:c.259-214del	NP_001317469.1:n.259-214del
XM_005270724.5:c.235-214del	XP_005270781.1:n.235-214del
NM_015506.3:c.430-214del MANE Select	NP_056321.2:n.430-214del
NM_001330540.2:c.259-214del	NP_001317469.1:n.259-214del