Canonical Allele Identifier: CA1554416538
Gene: CARTPT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719379_71719380delinsAG , CM000667.2:g.71719379_71719380delinsAG GRCh38
NC_000005.9:g.71015206_71015207delinsAG , CM000667.1:g.71015206_71015207delinsAG GRCh37
NC_000005.8:g.71050962_71050963delinsAG NCBI36
NG_015988.1:g.5217_5218delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.86_87delinsAG MANE Select ENSP00000296777.4:p.Glu29=
ENST00000296777.4:c.86_87delinsAG ENSP00000296777.4:p.Glu29=
NM_004291.3:c.86_87delinsAG NP_004282.1:p.Glu29=
NM_004291.4:c.86_87delinsAG MANE Select NP_004282.1:p.Glu29=
Search 100 bp 5'
Search 100 bp 3'