Canonical Allele Identifier: CA736190161
Gene: MMACHC HGNC NCBI

Linked Data

dbSNP Id: rs1385416872

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508261_45508262insATTGCTGAC , CM000663.2:g.45508261_45508262insATTGCTGAC GRCh38
NC_000001.10:g.45973933_45973934insATTGCTGAC , CM000663.1:g.45973933_45973934insATTGCTGAC GRCh37
NC_000001.9:g.45746520_45746521insATTGCTGAC NCBI36
NG_013378.1:g.13078_13079insATTGCTGAC

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.326_327insATTGCTGAC MANE Select ENSP00000383840.4:p.Pro109_Asn110insLeuLe...
ENST00000401061.8:c.326_327insATTGCTGAC ENSP00000383840.4:p.Pro109_Asn110insLeuLe...
ENST00000616135.1:c.155_156insATTGCTGAC ENSP00000478859.1:p.Pro52_Asn53insLeuLeuT...
NM_015506.2:c.326_327insATTGCTGAC NP_056321.2:p.Pro109_Asn110insLeuLeuThr
XM_005270724.3:c.131_132insATTGCTGAC XP_005270781.1:p.Pro44_Asn45insLeuLeuThr
XM_011541204.1:c.155_156insATTGCTGAC XP_011539506.1:p.Pro52_Asn53insLeuLeuThr
NM_001330540.1:c.155_156insATTGCTGAC NP_001317469.1:p.Pro52_Asn53insLeuLeuThr
XM_005270724.5:c.131_132insATTGCTGAC XP_005270781.1:p.Pro44_Asn45insLeuLeuThr
NM_015506.3:c.326_327insATTGCTGAC MANE Select NP_056321.2:p.Pro109_Asn110insLeuLeuThr
NM_001330540.2:c.155_156insATTGCTGAC NP_001317469.1:p.Pro52_Asn53insLeuLeuThr