Canonical Allele Identifier: CA60471535

Gene: STK39

Linked Data

• dbSNP Id: rs775396684
• MyVariant Identifiers: chr2:g.169041340G>T (hg19) ; chr2:g.168184830G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168184830G>T , CM000664.2:g.168184830G>T	GRCh38
NC_000002.11:g.169041340G>T , CM000664.1:g.169041340G>T	GRCh37
NC_000002.10:g.168749586G>T	NCBI36
NG_052783.1:g.67766C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697205.1:c.209-2740C>A	ENSP00000513185.1:n.209-2740C>A
ENST00000355999.5:c.209-2740C>A MANE Select	ENSP00000348278.4:n.209-2740C>A
ENST00000355999.4:c.209-2740C>A	ENSP00000348278.4:n.209-2740C>A
NM_013233.2:c.209-2740C>A	NP_037365.2:n.209-2740C>A
XM_005246465.2:c.209-2740C>A	XP_005246522.1:n.209-2740C>A
XM_011510966.1:c.209-2740C>A	XP_011509268.1:n.209-2740C>A
XM_011510967.1:c.209-2740C>A	XP_011509269.1:n.209-2740C>A
XM_011510968.1:c.209-2740C>A	XP_011509270.1:n.209-2740C>A
XM_017003813.2:c.209-2740C>A	XP_016859302.1:n.209-2740C>A
XM_017003814.2:c.209-2740C>A	XP_016859303.1:n.209-2740C>A
XM_017003815.2:c.-98-2740C>A	XP_016859304.1:n.-98-2740C>A
XM_017003816.2:c.209-2740C>A	XP_016859305.1:n.209-2740C>A
NM_013233.3:c.209-2740C>A MANE Select	NP_037365.2:n.209-2740C>A