Canonical Allele Identifier: CA1554416313
Gene: CARTPT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719281G= , CM000667.2:g.71719281G= GRCh38
NC_000005.9:g.71015108G= , CM000667.1:g.71015108G= GRCh37
NC_000005.8:g.71050864G= NCBI36
NG_015988.1:g.5119G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.-13G= MANE Select ENSP00000296777.4:n.-13G=
ENST00000296777.4:c.-13G= ENSP00000296777.4:n.-13G=
NM_004291.3:c.-13G= NP_004282.1:n.-13G=
NM_004291.4:c.-13G= MANE Select NP_004282.1:n.-13G=
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