Canonical Allele Identifier: CA2628214285
Gene: PATL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711246_44711320del , CM000677.2:g.44711246_44711320del GRCh38
NC_000015.9:g.45003444_45003518del , CM000677.1:g.45003444_45003518del GRCh37
NC_000015.8:g.42790736_42790810del NCBI36
NG_012920.1:g.4760_4834del
NG_012920.2:g.4770_4844del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682850.1:c.-553_-479del MANE Select ENSP00000508024.1:n.-553_-479del
XM_011521338.1:c.-553_-479del XP_011519640.1:n.-553_-479del
XM_011521339.1:c.-434_-360del XP_011519641.1:n.-434_-360del
XM_011521340.1:c.-375_-301del XP_011519642.1:n.-375_-301del
XM_011521343.1:c.-637_-563del XP_011519645.1:n.-637_-563del
XM_011521345.1:c.-608_-534del XP_011519647.1:n.-608_-534del
XM_011521338.3:c.-553_-479del XP_011519640.1:n.-553_-479del
XM_011521339.3:c.-434_-360del XP_011519641.1:n.-434_-360del
XM_011521340.3:c.-375_-301del XP_011519642.1:n.-375_-301del
XM_011521343.3:c.-637_-563del XP_011519645.1:n.-637_-563del
XM_011521345.3:c.-608_-534del XP_011519647.1:n.-608_-534del
NM_001387260.1:c.-76+13_-76+87del NP_001374189.1:n.-76+13_-76+87del
NM_001387261.1:c.-375_-301del NP_001374190.1:n.-375_-301del
NM_001387262.1:c.-643_-569del NP_001374191.1:n.-643_-569del
NM_001387263.1:c.-553_-479del MANE Select NP_001374192.1:n.-553_-479del