Canonical Allele Identifier: CA1554417000
Gene: CARTPT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719591T= , CM000667.2:g.71719591T= GRCh38
NC_000005.9:g.71015418T= , CM000667.1:g.71015418T= GRCh37
NC_000005.8:g.71051174T= NCBI36
NG_015988.1:g.5429T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.159+139T= MANE Select ENSP00000296777.4:n.159+139T=
ENST00000296777.4:c.159+139T= ENSP00000296777.4:n.159+139T=
ENST00000513096.1:n.13T=
NM_004291.3:c.159+139T= NP_004282.1:n.159+139T=
NM_004291.4:c.159+139T= MANE Select NP_004282.1:n.159+139T=
Search 100 bp 5'
Search 100 bp 3'