Canonical Allele Identifier: CA137277909

Gene: TULP1

Linked Data

• dbSNP Id: rs534847827
• gnomAD v2: 6-35467661-G-GGT
• gnomAD v3: 6-35499884-G-GGT
• gnomAD v4: 6-35499884-G-GGT
• MyVariant Identifiers: chr6:g.35467663_35467664insGT (hg19) ; chr6:g.35467661_35467662insGT (hg19) ; chr6:g.35499886_35499887insGT (hg38) ; chr6:g.35499884_35499885insGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35499898_35499899dup , CM000668.2:g.35499898_35499899dup	GRCh38
NC_000006.11:g.35467675_35467676dup , CM000668.1:g.35467675_35467676dup	GRCh37
NC_000006.10:g.35575653_35575654dup	NCBI36
NG_009077.1:g.17985_17986dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229771.11:c.1495+95_1495+96dup MANE Select	ENSP00000229771.6:n.1495+95_1495+96dup
ENST00000229771.10:c.1495+95_1495+96dup	ENSP00000229771.6:n.1495+95_1495+96dup
ENST00000322263.8:c.1336+95_1336+96dup	ENSP00000319414.4:n.1336+95_1336+96dup
ENST00000614066.4:c.1489+95_1489+96dup	ENSP00000477534.1:n.1489+95_1489+96dup
NM_001289395.1:c.1336+95_1336+96dup	NP_001276324.1:n.1336+95_1336+96dup
NM_003322.4:c.1495+95_1495+96dup	NP_003313.3:n.1495+95_1495+96dup
NM_003322.5:c.1495+95_1495+96dup	NP_003313.3:n.1495+95_1495+96dup
NM_003322.6:c.1495+95_1495+96dup MANE Select	NP_003313.3:n.1495+95_1495+96dup
NM_001289395.2:c.1336+95_1336+96dup	NP_001276324.1:n.1336+95_1336+96dup