Canonical Allele Identifier: CA2770630078

Gene: TULP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35500304_35500305insAGA , CM000668.2:g.35500304_35500305insAGA	GRCh38
NC_000006.11:g.35468081_35468082insAGA , CM000668.1:g.35468081_35468082insAGA	GRCh37
NC_000006.10:g.35576059_35576060insAGA	NCBI36
NG_009077.1:g.17566_17567insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229771.11:c.1324-153_1324-152insTCT MANE Select	ENSP00000229771.6:n.1324-153_1324-152insTCT
ENST00000229771.10:c.1324-153_1324-152insTCT	ENSP00000229771.6:n.1324-153_1324-152insTCT
ENST00000322263.8:c.1165-153_1165-152insTCT	ENSP00000319414.4:n.1165-153_1165-152insTCT
ENST00000495781.1:n.500-153_500-152insTCT
ENST00000614066.4:c.1318-153_1318-152insTCT	ENSP00000477534.1:n.1318-153_1318-152insTCT
NM_001289395.1:c.1165-153_1165-152insTCT	NP_001276324.1:n.1165-153_1165-152insTCT
NM_003322.4:c.1324-153_1324-152insTCT	NP_003313.3:n.1324-153_1324-152insTCT
NM_003322.5:c.1324-153_1324-152insTCT	NP_003313.3:n.1324-153_1324-152insTCT
NM_003322.6:c.1324-153_1324-152insTCT MANE Select	NP_003313.3:n.1324-153_1324-152insTCT
NM_001289395.2:c.1165-153_1165-152insTCT	NP_001276324.1:n.1165-153_1165-152insTCT