Canonical Allele Identifier: CA2770629921
Gene: TULP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35500257_35500258insAGA , CM000668.2:g.35500257_35500258insAGA GRCh38
NC_000006.11:g.35468034_35468035insAGA , CM000668.1:g.35468034_35468035insAGA GRCh37
NC_000006.10:g.35576012_35576013insAGA NCBI36
NG_009077.1:g.17613_17614insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000229771.11:c.1324-106_1324-105insTCT MANE Select ENSP00000229771.6:n.1324-106_1324-105insTCT
ENST00000229771.10:c.1324-106_1324-105insTCT ENSP00000229771.6:n.1324-106_1324-105insTCT
ENST00000322263.8:c.1165-106_1165-105insTCT ENSP00000319414.4:n.1165-106_1165-105insTCT
ENST00000495781.1:n.500-106_500-105insTCT
ENST00000614066.4:c.1318-106_1318-105insTCT ENSP00000477534.1:n.1318-106_1318-105insTCT
NM_001289395.1:c.1165-106_1165-105insTCT NP_001276324.1:n.1165-106_1165-105insTCT
NM_003322.4:c.1324-106_1324-105insTCT NP_003313.3:n.1324-106_1324-105insTCT
NM_003322.5:c.1324-106_1324-105insTCT NP_003313.3:n.1324-106_1324-105insTCT
NM_003322.6:c.1324-106_1324-105insTCT MANE Select NP_003313.3:n.1324-106_1324-105insTCT
NM_001289395.2:c.1165-106_1165-105insTCT NP_001276324.1:n.1165-106_1165-105insTCT