Canonical Allele Identifier: CA1620921939
Gene: TULP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35503627G= , CM000668.2:g.35503627G= GRCh38
NC_000006.11:g.35471404G= , CM000668.1:g.35471404G= GRCh37
NC_000006.10:g.35579382G= NCBI36
NG_009077.1:g.14244C=

Transcript Alleles

HGVS Amino-acid change
ENST00000229771.11:c.1255C= MANE Select ENSP00000229771.6:p.Arg419=
ENST00000229771.10:c.1255C= ENSP00000229771.6:p.Arg419=
ENST00000322263.8:c.1096C= ENSP00000319414.4:p.Arg366=
ENST00000495781.1:n.431C=
ENST00000496434.5:n.272C=
ENST00000614066.4:c.1249C= ENSP00000477534.1:p.Arg417=
NM_001289395.1:c.1096C= NP_001276324.1:p.Arg366=
NM_003322.4:c.1255C= NP_003313.3:p.Arg419=
NM_003322.5:c.1255C= NP_003313.3:p.Arg419=
NM_003322.6:c.1255C= MANE Select NP_003313.3:p.Arg419=
NM_001289395.2:c.1096C= NP_001276324.1:p.Arg366=