Canonical Allele Identifier: CA449942455

Gene: TULP1

Linked Data

• ClinVar Variation Id: 3017666
• ClinVar RCV Id: RCV003874265
• dbSNP Id: rs1361647117
• MyVariant Identifiers: chr6:g.35467897G>A (hg19) ; chr6:g.35500120G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35500120G>A , CM000668.2:g.35500120G>A	GRCh38
NC_000006.11:g.35467897G>A , CM000668.1:g.35467897G>A	GRCh37
NC_000006.10:g.35575875G>A	NCBI36
NG_009077.1:g.17751C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229771.11:c.1356C>T MANE Select	ENSP00000229771.6:p.Asn452=
ENST00000229771.10:c.1356C>T	ENSP00000229771.6:p.Asn452=
ENST00000322263.8:c.1197C>T	ENSP00000319414.4:p.Asn399=
ENST00000495781.1:n.532C>T
ENST00000614066.4:c.1350C>T	ENSP00000477534.1:p.Asn450=
NM_001289395.1:c.1197C>T	NP_001276324.1:p.Asn399=
NM_003322.4:c.1356C>T	NP_003313.3:p.Asn452=
NM_003322.5:c.1356C>T	NP_003313.3:p.Asn452=
NM_003322.6:c.1356C>T MANE Select	NP_003313.3:p.Asn452=
NM_001289395.2:c.1197C>T	NP_001276324.1:p.Asn399=