Canonical Allele Identifier: CA3772613
Gene: TULP1 HGNC NCBI

Linked Data

dbSNP Id: rs762666014
gnomAD v2: 6-35471405-G-A
gnomAD v4: 6-35503628-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35503628G>A , CM000668.2:g.35503628G>A GRCh38
NC_000006.11:g.35471405G>A , CM000668.1:g.35471405G>A GRCh37
NC_000006.10:g.35579383G>A NCBI36
NG_009077.1:g.14243C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000229771.11:c.1254C>T MANE Select ENSP00000229771.6:p.Pro418=
ENST00000229771.10:c.1254C>T ENSP00000229771.6:p.Pro418=
ENST00000322263.8:c.1095C>T ENSP00000319414.4:p.Pro365=
ENST00000495781.1:n.430C>T
ENST00000496434.5:n.271C>T
ENST00000614066.4:c.1248C>T ENSP00000477534.1:p.Pro416=
NM_001289395.1:c.1095C>T NP_001276324.1:p.Pro365=
NM_003322.4:c.1254C>T NP_003313.3:p.Pro418=
NM_003322.5:c.1254C>T NP_003313.3:p.Pro418=
NM_003322.6:c.1254C>T MANE Select NP_003313.3:p.Pro418=
NM_001289395.2:c.1095C>T NP_001276324.1:p.Pro365=