Canonical Allele Identifier: CA2770629900

Gene: TULP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35500250_35500251insAGA , CM000668.2:g.35500250_35500251insAGA	GRCh38
NC_000006.11:g.35468027_35468028insAGA , CM000668.1:g.35468027_35468028insAGA	GRCh37
NC_000006.10:g.35576005_35576006insAGA	NCBI36
NG_009077.1:g.17620_17621insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229771.11:c.1324-99_1324-98insTCT MANE Select	ENSP00000229771.6:n.1324-99_1324-98insTCT
ENST00000229771.10:c.1324-99_1324-98insTCT	ENSP00000229771.6:n.1324-99_1324-98insTCT
ENST00000322263.8:c.1165-99_1165-98insTCT	ENSP00000319414.4:n.1165-99_1165-98insTCT
ENST00000495781.1:n.500-99_500-98insTCT
ENST00000614066.4:c.1318-99_1318-98insTCT	ENSP00000477534.1:n.1318-99_1318-98insTCT
NM_001289395.1:c.1165-99_1165-98insTCT	NP_001276324.1:n.1165-99_1165-98insTCT
NM_003322.4:c.1324-99_1324-98insTCT	NP_003313.3:n.1324-99_1324-98insTCT
NM_003322.5:c.1324-99_1324-98insTCT	NP_003313.3:n.1324-99_1324-98insTCT
NM_003322.6:c.1324-99_1324-98insTCT MANE Select	NP_003313.3:n.1324-99_1324-98insTCT
NM_001289395.2:c.1165-99_1165-98insTCT	NP_001276324.1:n.1165-99_1165-98insTCT