Canonical Allele Identifier: CA2770630022

Gene: TULP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35500281_35500282insAGA , CM000668.2:g.35500281_35500282insAGA	GRCh38
NC_000006.11:g.35468058_35468059insAGA , CM000668.1:g.35468058_35468059insAGA	GRCh37
NC_000006.10:g.35576036_35576037insAGA	NCBI36
NG_009077.1:g.17589_17590insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229771.11:c.1324-130_1324-129insTCT MANE Select	ENSP00000229771.6:n.1324-130_1324-129insTCT
ENST00000229771.10:c.1324-130_1324-129insTCT	ENSP00000229771.6:n.1324-130_1324-129insTCT
ENST00000322263.8:c.1165-130_1165-129insTCT	ENSP00000319414.4:n.1165-130_1165-129insTCT
ENST00000495781.1:n.500-130_500-129insTCT
ENST00000614066.4:c.1318-130_1318-129insTCT	ENSP00000477534.1:n.1318-130_1318-129insTCT
NM_001289395.1:c.1165-130_1165-129insTCT	NP_001276324.1:n.1165-130_1165-129insTCT
NM_003322.4:c.1324-130_1324-129insTCT	NP_003313.3:n.1324-130_1324-129insTCT
NM_003322.5:c.1324-130_1324-129insTCT	NP_003313.3:n.1324-130_1324-129insTCT
NM_003322.6:c.1324-130_1324-129insTCT MANE Select	NP_003313.3:n.1324-130_1324-129insTCT
NM_001289395.2:c.1165-130_1165-129insTCT	NP_001276324.1:n.1165-130_1165-129insTCT