Canonical Allele Identifier: CA2674169339
Gene: CARTPT HGNC NCBI

Linked Data

gnomAD v4: 5-71719595-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719595A>T , CM000667.2:g.71719595A>T GRCh38
NC_000005.9:g.71015422A>T , CM000667.1:g.71015422A>T GRCh37
NC_000005.8:g.71051178A>T NCBI36
NG_015988.1:g.5433A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.159+143A>T MANE Select ENSP00000296777.4:n.159+143A>T
ENST00000296777.4:c.159+143A>T ENSP00000296777.4:n.159+143A>T
ENST00000513096.1:n.17A>T
NM_004291.3:c.159+143A>T NP_004282.1:n.159+143A>T
NM_004291.4:c.159+143A>T MANE Select NP_004282.1:n.159+143A>T
Search 100 bp 5'
Search 100 bp 3'