Canonical Allele Identifier: CA1554417136
Gene: CARTPT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719691A= , CM000667.2:g.71719691A= GRCh38
NC_000005.9:g.71015518A= , CM000667.1:g.71015518A= GRCh37
NC_000005.8:g.71051274A= NCBI36
NG_015988.1:g.5529A=

Transcript Alleles

HGVS Amino-acid change
ENST00000296777.5:c.160-189A= MANE Select ENSP00000296777.4:n.160-189A=
ENST00000296777.4:c.160-189A= ENSP00000296777.4:n.160-189A=
ENST00000513096.1:n.113A=
NM_004291.3:c.160-189A= NP_004282.1:n.160-189A=
NM_004291.4:c.160-189A= MANE Select NP_004282.1:n.160-189A=
Search 100 bp 5'
Search 100 bp 3'