Canonical Allele Identifier: CA969359895
Gene: GATM HGNC NCBI

Linked Data

dbSNP Id: rs1889895253

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45393653_45393654del , CM000677.2:g.45393653_45393654del GRCh38
NC_000015.9:g.45685851_45685852del , CM000677.1:g.45685851_45685852del GRCh37
NC_000015.8:g.43473143_43473144del NCBI36
NG_011674.2:g.13665_13666del

Transcript Alleles

HGVS Amino-acid Change
ENST00000458245.5:n.640+3269_640+3270del
ENST00000527933.2:n.512+2514_512+2515del
ENST00000560538.1:n.338+3269_338+3270del
ENST00000561148.5:c.-319+3269_-319+3270del ENSP00000453860.1:n.-319+3269_-319+3270del
XM_011521450.1:c.31+3269_31+3270del XP_011519752.1:n.31+3269_31+3270del
NM_001321015.1:c.-395+3269_-395+3270del NP_001307944.1:n.-395+3269_-395+3270del
NM_001321015.2:c.-395+3269_-395+3270del NP_001307944.1:n.-395+3269_-395+3270del