Canonical Allele Identifier: CA1554417131
Gene: CARTPT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719684G= , CM000667.2:g.71719684G= GRCh38
NC_000005.9:g.71015511G= , CM000667.1:g.71015511G= GRCh37
NC_000005.8:g.71051267G= NCBI36
NG_015988.1:g.5522G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.160-196G= MANE Select ENSP00000296777.4:n.160-196G=
ENST00000296777.4:c.160-196G= ENSP00000296777.4:n.160-196G=
ENST00000513096.1:n.106G=
NM_004291.3:c.160-196G= NP_004282.1:n.160-196G=
NM_004291.4:c.160-196G= MANE Select NP_004282.1:n.160-196G=
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