Canonical Allele Identifier: CA2578331742
Gene: CARTPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719792del , CM000667.2:g.71719792del GRCh38
NC_000005.9:g.71015619del , CM000667.1:g.71015619del GRCh37
NC_000005.8:g.71051375del NCBI36
NG_015988.1:g.5630del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.160-88del MANE Select ENSP00000296777.4:n.160-88del
ENST00000296777.4:c.160-88del ENSP00000296777.4:n.160-88del
ENST00000513096.1:n.214del
NM_004291.3:c.160-88del NP_004282.1:n.160-88del
NM_004291.4:c.160-88del MANE Select NP_004282.1:n.160-88del