Canonical Allele Identifier: CA363778969
Gene: TULP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.35467916A>G (hg19) chr6:g.35500139A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35500139A>G , CM000668.2:g.35500139A>G GRCh38
NC_000006.11:g.35467916A>G , CM000668.1:g.35467916A>G GRCh37
NC_000006.10:g.35575894A>G NCBI36
NG_009077.1:g.17732T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000229771.11:c.1337T>C MANE Select ENSP00000229771.6:p.Leu446Pro
ENST00000229771.10:c.1337T>C ENSP00000229771.6:p.Leu446Pro
ENST00000322263.8:c.1178T>C ENSP00000319414.4:p.Leu393Pro
ENST00000495781.1:n.513T>C
ENST00000614066.4:c.1331T>C ENSP00000477534.1:p.Leu444Pro
NM_001289395.1:c.1178T>C NP_001276324.1:p.Leu393Pro
NM_003322.4:c.1337T>C NP_003313.3:p.Leu446Pro
NM_003322.5:c.1337T>C NP_003313.3:p.Leu446Pro
NM_003322.6:c.1337T>C MANE Select NP_003313.3:p.Leu446Pro
NM_001289395.2:c.1178T>C NP_001276324.1:p.Leu393Pro
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