Canonical Allele Identifier: CA1620929037
Gene: TULP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35500071T= , CM000668.2:g.35500071T= GRCh38
NC_000006.11:g.35467848T= , CM000668.1:g.35467848T= GRCh37
NC_000006.10:g.35575826T= NCBI36
NG_009077.1:g.17800A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000229771.11:c.1405A= MANE Select ENSP00000229771.6:p.Asn469=
ENST00000229771.10:c.1405A= ENSP00000229771.6:p.Asn469=
ENST00000322263.8:c.1246A= ENSP00000319414.4:p.Asn416=
ENST00000495781.1:n.581A=
ENST00000614066.4:c.1399A= ENSP00000477534.1:p.Asn467=
NM_001289395.1:c.1246A= NP_001276324.1:p.Asn416=
NM_003322.4:c.1405A= NP_003313.3:p.Asn469=
NM_003322.5:c.1405A= NP_003313.3:p.Asn469=
NM_003322.6:c.1405A= MANE Select NP_003313.3:p.Asn469=
NM_001289395.2:c.1246A= NP_001276324.1:p.Asn416=