Canonical Allele Identifier: CA360104500
Gene: CARTPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719454T>C , CM000667.2:g.71719454T>C GRCh38
NC_000005.9:g.71015281T>C , CM000667.1:g.71015281T>C GRCh37
NC_000005.8:g.71051037T>C NCBI36
NG_015988.1:g.5292T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.159+2T>C MANE Select ENSP00000296777.4:n.159+2T>C
ENST00000296777.4:c.159+2T>C ENSP00000296777.4:n.159+2T>C
NM_004291.3:c.159+2T>C NP_004282.1:n.159+2T>C
NM_004291.4:c.159+2T>C MANE Select NP_004282.1:n.159+2T>C