Canonical Allele Identifier: CA363778526
Gene: TULP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.35467787T>G (hg19) chr6:g.35500010T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35500010T>G , CM000668.2:g.35500010T>G GRCh38
NC_000006.11:g.35467787T>G , CM000668.1:g.35467787T>G GRCh37
NC_000006.10:g.35575765T>G NCBI36
NG_009077.1:g.17861A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000229771.11:c.1466A>C MANE Select ENSP00000229771.6:p.Lys489Thr
ENST00000229771.10:c.1466A>C ENSP00000229771.6:p.Lys489Thr
ENST00000322263.8:c.1307A>C ENSP00000319414.4:p.Lys436Thr
ENST00000614066.4:c.1460A>C ENSP00000477534.1:p.Lys487Thr
NM_001289395.1:c.1307A>C NP_001276324.1:p.Lys436Thr
NM_003322.4:c.1466A>C NP_003313.3:p.Lys489Thr
NM_003322.5:c.1466A>C NP_003313.3:p.Lys489Thr
NM_003322.6:c.1466A>C MANE Select NP_003313.3:p.Lys489Thr
NM_001289395.2:c.1307A>C NP_001276324.1:p.Lys436Thr
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