Canonical Allele Identifier: CA1554416474
Gene: CARTPT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719353A= , CM000667.2:g.71719353A= GRCh38
NC_000005.9:g.71015180A= , CM000667.1:g.71015180A= GRCh37
NC_000005.8:g.71050936A= NCBI36
NG_015988.1:g.5191A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.60A= MANE Select ENSP00000296777.4:p.Leu20=
ENST00000296777.4:c.60A= ENSP00000296777.4:p.Leu20=
NM_004291.3:c.60A= NP_004282.1:p.Leu20=
NM_004291.4:c.60A= MANE Select NP_004282.1:p.Leu20=
Search 100 bp 5'
Search 100 bp 3'