Canonical Allele Identifier: CA11036658
Gene: STK39 HGNC NCBI

Linked Data

dbSNP Id: rs6749447

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168184876T>G , CM000664.2:g.168184876T>G GRCh38
NC_000002.11:g.169041386T>G , CM000664.1:g.169041386T>G GRCh37
NC_000002.10:g.168749632T>G NCBI36
NG_052783.1:g.67720A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000355999.5:c.209-2786A>C MANE Select ENSP00000348278.4:n.209-2786A>C
ENST00000355999.4:c.209-2786A>C ENSP00000348278.4:n.209-2786A>C
NM_013233.2:c.209-2786A>C NP_037365.2:n.209-2786A>C
XM_005246465.2:c.209-2786A>C XP_005246522.1:n.209-2786A>C
XM_011510966.1:c.209-2786A>C XP_011509268.1:n.209-2786A>C
XM_011510967.1:c.209-2786A>C XP_011509269.1:n.209-2786A>C
XM_011510968.1:c.209-2786A>C XP_011509270.1:n.209-2786A>C
XM_017003813.2:c.209-2786A>C XP_016859302.1:n.209-2786A>C
XM_017003814.2:c.209-2786A>C XP_016859303.1:n.209-2786A>C
XM_017003815.2:c.-98-2786A>C XP_016859304.1:n.-98-2786A>C
XM_017003816.2:c.209-2786A>C XP_016859305.1:n.209-2786A>C
NM_013233.3:c.209-2786A>C MANE Select NP_037365.2:n.209-2786A>C