Canonical Allele Identifier: CA2770629996

Gene: TULP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35500270_35500271insAGA , CM000668.2:g.35500270_35500271insAGA	GRCh38
NC_000006.11:g.35468047_35468048insAGA , CM000668.1:g.35468047_35468048insAGA	GRCh37
NC_000006.10:g.35576025_35576026insAGA	NCBI36
NG_009077.1:g.17600_17601insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229771.11:c.1324-119_1324-118insTCT MANE Select	ENSP00000229771.6:n.1324-119_1324-118insTCT
ENST00000229771.10:c.1324-119_1324-118insTCT	ENSP00000229771.6:n.1324-119_1324-118insTCT
ENST00000322263.8:c.1165-119_1165-118insTCT	ENSP00000319414.4:n.1165-119_1165-118insTCT
ENST00000495781.1:n.500-119_500-118insTCT
ENST00000614066.4:c.1318-119_1318-118insTCT	ENSP00000477534.1:n.1318-119_1318-118insTCT
NM_001289395.1:c.1165-119_1165-118insTCT	NP_001276324.1:n.1165-119_1165-118insTCT
NM_003322.4:c.1324-119_1324-118insTCT	NP_003313.3:n.1324-119_1324-118insTCT
NM_003322.5:c.1324-119_1324-118insTCT	NP_003313.3:n.1324-119_1324-118insTCT
NM_003322.6:c.1324-119_1324-118insTCT MANE Select	NP_003313.3:n.1324-119_1324-118insTCT
NM_001289395.2:c.1165-119_1165-118insTCT	NP_001276324.1:n.1165-119_1165-118insTCT