Canonical Allele Identifier: CA360104212
Gene: CARTPT HGNC NCBI

Linked Data

dbSNP Id: rs1748653841
MyVariant Identifiers: chr5:g.71015139A>T (hg19) chr5:g.71719312A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719312A>T , CM000667.2:g.71719312A>T GRCh38
NC_000005.9:g.71015139A>T , CM000667.1:g.71015139A>T GRCh37
NC_000005.8:g.71050895A>T NCBI36
NG_015988.1:g.5150A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.19A>T MANE Select ENSP00000296777.4:p.Arg7Trp
ENST00000296777.4:c.19A>T ENSP00000296777.4:p.Arg7Trp
NM_004291.3:c.19A>T NP_004282.1:p.Arg7Trp
NM_004291.4:c.19A>T MANE Select NP_004282.1:p.Arg7Trp
Search 100 bp 5'
Search 100 bp 3'