Canonical Allele Identifier: CA2838234929
Gene: TSKS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49761931_49761932dup , CM000681.2:g.49761931_49761932dup GRCh38
NC_000019.9:g.50265188_50265189dup , CM000681.1:g.50265188_50265189dup GRCh37
NC_000019.8:g.54957000_54957001dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000246801.8:c.399+75_399+76dup MANE Select ENSP00000246801.2:n.399+75_399+76dup
ENST00000246801.7:c.399+75_399+76dup ENSP00000246801.2:n.399+75_399+76dup
NM_021733.1:c.399+75_399+76dup NP_068379.1:n.399+75_399+76dup
XM_005259130.2:c.399+75_399+76dup XP_005259187.1:n.399+75_399+76dup
XM_011527201.1:c.399+75_399+76dup XP_011525503.1:n.399+75_399+76dup
XM_011527202.1:c.399+75_399+76dup XP_011525504.1:n.399+75_399+76dup
XM_011527203.1:c.399+75_399+76dup XP_011525505.1:n.399+75_399+76dup
XM_011527203.2:c.399+75_399+76dup XP_011525505.1:n.399+75_399+76dup
NM_021733.2:c.399+75_399+76dup MANE Select NP_068379.1:n.399+75_399+76dup