Canonical Allele Identifier: CA2674169321
Gene: CARTPT HGNC NCBI

Linked Data

gnomAD v4: 5-71719581-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719581A>G , CM000667.2:g.71719581A>G GRCh38
NC_000005.9:g.71015408A>G , CM000667.1:g.71015408A>G GRCh37
NC_000005.8:g.71051164A>G NCBI36
NG_015988.1:g.5419A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.159+129A>G MANE Select ENSP00000296777.4:n.159+129A>G
ENST00000296777.4:c.159+129A>G ENSP00000296777.4:n.159+129A>G
ENST00000513096.1:n.3A>G
NM_004291.3:c.159+129A>G NP_004282.1:n.159+129A>G
NM_004291.4:c.159+129A>G MANE Select NP_004282.1:n.159+129A>G
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