Canonical Allele Identifier: CA363778929
Gene: TULP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35500121T>G , CM000668.2:g.35500121T>G GRCh38
NC_000006.11:g.35467898T>G , CM000668.1:g.35467898T>G GRCh37
NC_000006.10:g.35575876T>G NCBI36
NG_009077.1:g.17750A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000229771.11:c.1355A>C MANE Select ENSP00000229771.6:p.Asn452Thr
ENST00000229771.10:c.1355A>C ENSP00000229771.6:p.Asn452Thr
ENST00000322263.8:c.1196A>C ENSP00000319414.4:p.Asn399Thr
ENST00000495781.1:n.531A>C
ENST00000614066.4:c.1349A>C ENSP00000477534.1:p.Asn450Thr
NM_001289395.1:c.1196A>C NP_001276324.1:p.Asn399Thr
NM_003322.4:c.1355A>C NP_003313.3:p.Asn452Thr
NM_003322.5:c.1355A>C NP_003313.3:p.Asn452Thr
NM_003322.6:c.1355A>C MANE Select NP_003313.3:p.Asn452Thr
NM_001289395.2:c.1196A>C NP_001276324.1:p.Asn399Thr