Canonical Allele Identifier: CA449942463
Gene: TULP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.35467906G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35500129G>A , CM000668.2:g.35500129G>A GRCh38
NC_000006.11:g.35467906G>A , CM000668.1:g.35467906G>A GRCh37
NC_000006.10:g.35575884G>A NCBI36
NG_009077.1:g.17742C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000229771.11:c.1347C>T MANE Select ENSP00000229771.6:p.Arg449=
ENST00000229771.10:c.1347C>T ENSP00000229771.6:p.Arg449=
ENST00000322263.8:c.1188C>T ENSP00000319414.4:p.Arg396=
ENST00000495781.1:n.523C>T
ENST00000614066.4:c.1341C>T ENSP00000477534.1:p.Arg447=
NM_001289395.1:c.1188C>T NP_001276324.1:p.Arg396=
NM_003322.4:c.1347C>T NP_003313.3:p.Arg449=
NM_003322.5:c.1347C>T NP_003313.3:p.Arg449=
NM_003322.6:c.1347C>T MANE Select NP_003313.3:p.Arg449=
NM_001289395.2:c.1188C>T NP_001276324.1:p.Arg396=