Canonical Allele Identifier: CA1620928862
Gene: TULP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35499898T= , CM000668.2:g.35499898T= GRCh38
NC_000006.11:g.35467675T= , CM000668.1:g.35467675T= GRCh37
NC_000006.10:g.35575653T= NCBI36
NG_009077.1:g.17973A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000229771.11:c.1495+83A= MANE Select ENSP00000229771.6:n.1495+83A=
ENST00000229771.10:c.1495+83A= ENSP00000229771.6:n.1495+83A=
ENST00000322263.8:c.1336+83A= ENSP00000319414.4:n.1336+83A=
ENST00000614066.4:c.1489+83A= ENSP00000477534.1:n.1489+83A=
NM_001289395.1:c.1336+83A= NP_001276324.1:n.1336+83A=
NM_003322.4:c.1495+83A= NP_003313.3:n.1495+83A=
NM_003322.5:c.1495+83A= NP_003313.3:n.1495+83A=
NM_003322.6:c.1495+83A= MANE Select NP_003313.3:n.1495+83A=
NM_001289395.2:c.1336+83A= NP_001276324.1:n.1336+83A=