Canonical Allele Identifier: CA2674169252
Gene: CARTPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719486_71719487insGAC , CM000667.2:g.71719486_71719487insGAC GRCh38
NC_000005.9:g.71015313_71015314insGAC , CM000667.1:g.71015313_71015314insGAC GRCh37
NC_000005.8:g.71051069_71051070insGAC NCBI36
NG_015988.1:g.5324_5325insGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.159+34_159+35insGAC MANE Select ENSP00000296777.4:n.159+34_159+35insGAC
ENST00000296777.4:c.159+34_159+35insGAC ENSP00000296777.4:n.159+34_159+35insGAC
NM_004291.3:c.159+34_159+35insGAC NP_004282.1:n.159+34_159+35insGAC
NM_004291.4:c.159+34_159+35insGAC MANE Select NP_004282.1:n.159+34_159+35insGAC