Canonical Allele Identifier: CA736185341

Gene: MMACHC

Linked Data

• dbSNP Id: rs1175995418
• MyVariant Identifiers: chr1:g.45966404_45966407del (hg19) ; chr1:g.45500732_45500735del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45500735_45500738del , CM000663.2:g.45500735_45500738del	GRCh38
NC_000001.10:g.45966407_45966410del , CM000663.1:g.45966407_45966410del	GRCh37
NC_000001.9:g.45738994_45738997del	NCBI36
NG_013378.1:g.5552_5555del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.81+322_81+325del MANE Select	ENSP00000383840.4:n.81+322_81+325del
ENST00000401061.8:c.81+322_81+325del	ENSP00000383840.4:n.81+322_81+325del
ENST00000616135.1:c.-91+322_-91+325del	ENSP00000478859.1:n.-91+322_-91+325del
NM_015506.2:c.81+322_81+325del	NP_056321.2:n.81+322_81+325del
XM_005270724.3:c.81+322_81+325del	XP_005270781.1:n.81+322_81+325del
XM_011541204.1:c.-142+322_-142+325del	XP_011539506.1:n.-142+322_-142+325del
NM_001330540.1:c.-142+322_-142+325del	NP_001317469.1:n.-142+322_-142+325del
XM_005270724.5:c.81+322_81+325del	XP_005270781.1:n.81+322_81+325del
NM_015506.3:c.81+322_81+325del MANE Select	NP_056321.2:n.81+322_81+325del
NM_001330540.2:c.-142+322_-142+325del	NP_001317469.1:n.-142+322_-142+325del