Canonical Allele Identifier: CA813670398
Gene: CARTPT HGNC NCBI

Linked Data

dbSNP Id: rs1026298284
MyVariant Identifiers: chr5:g.71015334T>A (hg19) chr5:g.71719507T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719507T>A , CM000667.2:g.71719507T>A GRCh38
NC_000005.9:g.71015334T>A , CM000667.1:g.71015334T>A GRCh37
NC_000005.8:g.71051090T>A NCBI36
NG_015988.1:g.5345T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.159+55T>A MANE Select ENSP00000296777.4:n.159+55T>A
ENST00000296777.4:c.159+55T>A ENSP00000296777.4:n.159+55T>A
NM_004291.3:c.159+55T>A NP_004282.1:n.159+55T>A
NM_004291.4:c.159+55T>A MANE Select NP_004282.1:n.159+55T>A
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