Canonical Allele Identifier: CA449942477
Gene: TULP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.35467915C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35500138C>A , CM000668.2:g.35500138C>A GRCh38
NC_000006.11:g.35467915C>A , CM000668.1:g.35467915C>A GRCh37
NC_000006.10:g.35575893C>A NCBI36
NG_009077.1:g.17733G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000229771.11:c.1338G>T MANE Select ENSP00000229771.6:p.Leu446=
ENST00000229771.10:c.1338G>T ENSP00000229771.6:p.Leu446=
ENST00000322263.8:c.1179G>T ENSP00000319414.4:p.Leu393=
ENST00000495781.1:n.514G>T
ENST00000614066.4:c.1332G>T ENSP00000477534.1:p.Leu444=
NM_001289395.1:c.1179G>T NP_001276324.1:p.Leu393=
NM_003322.4:c.1338G>T NP_003313.3:p.Leu446=
NM_003322.5:c.1338G>T NP_003313.3:p.Leu446=
NM_003322.6:c.1338G>T MANE Select NP_003313.3:p.Leu446=
NM_001289395.2:c.1179G>T NP_001276324.1:p.Leu393=