Canonical Allele Identifier: CA2766960269
Gene: CARTPT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719283G>T , CM000667.2:g.71719283G>T GRCh38
NC_000005.9:g.71015110G>T , CM000667.1:g.71015110G>T GRCh37
NC_000005.8:g.71050866G>T NCBI36
NG_015988.1:g.5121G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.-11G>T MANE Select ENSP00000296777.4:n.-11G>T
ENST00000296777.4:c.-11G>T ENSP00000296777.4:n.-11G>T
NM_004291.3:c.-11G>T NP_004282.1:n.-11G>T
NM_004291.4:c.-11G>T MANE Select NP_004282.1:n.-11G>T
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