Canonical Allele Identifier: CA1305769381
Gene: STK39 HGNC NCBI

Linked Data

dbSNP Id: rs1177069559
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.167954869C>A , CM000664.2:g.167954869C>A GRCh38
NC_000002.11:g.168811379C>A , CM000664.1:g.168811379C>A GRCh37
NC_000002.10:g.168519625C>A NCBI36
NG_052783.1:g.297727G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000697205.1:c.2202G>T ENSP00000513185.1:n.2202G>T
ENST00000355999.5:c.*627G>T MANE Select ENSP00000348278.4:n.*627G>T
ENST00000355999.4:c.*627G>T ENSP00000348278.4:n.*627G>T
ENST00000487143.5:n.1365G>T
NM_013233.2:c.*627G>T NP_037365.2:n.*627G>T
XM_005246465.2:c.*627G>T XP_005246522.1:n.*627G>T
XM_011510966.1:c.*627G>T XP_011509268.1:n.*627G>T
XM_011510967.1:c.*627G>T XP_011509269.1:n.*627G>T
NM_013233.3:c.*627G>T MANE Select NP_037365.2:n.*627G>T
Search 100 bp 5'
Search 100 bp 3'