Canonical Allele Identifier: CA363778972
Gene: TULP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35500140G>T , CM000668.2:g.35500140G>T GRCh38
NC_000006.11:g.35467917G>T , CM000668.1:g.35467917G>T GRCh37
NC_000006.10:g.35575895G>T NCBI36
NG_009077.1:g.17731C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000229771.11:c.1336C>A MANE Select ENSP00000229771.6:p.Leu446Met
ENST00000229771.10:c.1336C>A ENSP00000229771.6:p.Leu446Met
ENST00000322263.8:c.1177C>A ENSP00000319414.4:p.Leu393Met
ENST00000495781.1:n.512C>A
ENST00000614066.4:c.1330C>A ENSP00000477534.1:p.Leu444Met
NM_001289395.1:c.1177C>A NP_001276324.1:p.Leu393Met
NM_003322.4:c.1336C>A NP_003313.3:p.Leu446Met
NM_003322.5:c.1336C>A NP_003313.3:p.Leu446Met
NM_003322.6:c.1336C>A MANE Select NP_003313.3:p.Leu446Met
NM_001289395.2:c.1177C>A NP_001276324.1:p.Leu393Met