Canonical Allele Identifier: CA2674169462
Gene: CARTPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719675_71719676insGCCCC , CM000667.2:g.71719675_71719676insGCCCC GRCh38
NC_000005.9:g.71015502_71015503insGCCCC , CM000667.1:g.71015502_71015503insGCCCC GRCh37
NC_000005.8:g.71051258_71051259insGCCCC NCBI36
NG_015988.1:g.5513_5514insGCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.160-205_160-204insGCCCC MANE Select ENSP00000296777.4:n.160-205_160-204insGCCCC
ENST00000296777.4:c.160-205_160-204insGCCCC ENSP00000296777.4:n.160-205_160-204insGCCCC
ENST00000513096.1:n.97_98insGCCCC
NM_004291.3:c.160-205_160-204insGCCCC NP_004282.1:n.160-205_160-204insGCCCC
NM_004291.4:c.160-205_160-204insGCCCC MANE Select NP_004282.1:n.160-205_160-204insGCCCC