Canonical Allele Identifier: CA2674169463
Gene: CARTPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719676del , CM000667.2:g.71719676del GRCh38
NC_000005.9:g.71015503del , CM000667.1:g.71015503del GRCh37
NC_000005.8:g.71051259del NCBI36
NG_015988.1:g.5514del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.160-204del MANE Select ENSP00000296777.4:n.160-204del
ENST00000296777.4:c.160-204del ENSP00000296777.4:n.160-204del
ENST00000513096.1:n.98del
NM_004291.3:c.160-204del NP_004282.1:n.160-204del
NM_004291.4:c.160-204del MANE Select NP_004282.1:n.160-204del