Canonical Allele Identifier: CA16172985

Gene: STK32B

Linked Data

• dbSNP Id: rs2008242
• gnomAD v2: 4-5221538-G-C
• gnomAD v3: 4-5219811-G-C
• gnomAD v4: 4-5219811-G-C
• MyVariant Identifiers: chr4:g.5221538G>C (hg19) ; chr4:g.5219811G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5219811G>C , CM000666.2:g.5219811G>C	GRCh38
NC_000004.11:g.5221538G>C , CM000666.1:g.5221538G>C	GRCh37
NC_000004.10:g.5272439G>C	NCBI36
NG_051593.1:g.173489G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000282908.10:c.260+51361G>C MANE Select	ENSP00000282908.5:n.260+51361G>C
ENST00000282908.9:c.260+51361G>C	ENSP00000282908.5:n.260+51361G>C
ENST00000505508.5:n.56+5514G>C
ENST00000510398.1:c.119+51361G>C	ENSP00000420984.1:n.119+51361G>C
ENST00000512018.5:c.*214+51361G>C	ENSP00000422820.1:n.*214+51361G>C
ENST00000512636.5:c.119+51361G>C	ENSP00000423209.1:n.119+51361G>C
ENST00000513705.5:n.158+15575G>C
NM_001306082.1:c.119+51361G>C	NP_001293011.1:n.119+51361G>C
NM_018401.1:c.260+51361G>C	NP_060871.1:n.260+51361G>C
NM_018401.2:c.260+51361G>C	NP_060871.1:n.260+51361G>C
XM_011513497.1:c.260+51361G>C	XP_011511799.1:n.260+51361G>C
XM_011513498.1:c.260+51361G>C	XP_011511800.1:n.260+51361G>C
XM_011513499.1:c.260+51361G>C	XP_011511801.1:n.260+51361G>C
XM_011513500.1:c.260+51361G>C	XP_011511802.1:n.260+51361G>C
XM_011513502.1:c.260+51361G>C	XP_011511804.1:n.260+51361G>C
NM_001345969.1:c.260+51361G>C	NP_001332898.1:n.260+51361G>C
XM_017008374.1:c.119+51361G>C	XP_016863863.1:n.119+51361G>C
XM_017008375.1:c.119+51361G>C	XP_016863864.1:n.119+51361G>C
XM_017008376.1:c.119+51361G>C	XP_016863865.1:n.119+51361G>C
XM_024454131.1:c.119+51361G>C	XP_024309899.1:n.119+51361G>C
NM_018401.3:c.260+51361G>C MANE Select	NP_060871.1:n.260+51361G>C
NM_001306082.2:c.119+51361G>C	NP_001293011.1:n.119+51361G>C
NM_001345969.2:c.260+51361G>C	NP_001332898.1:n.260+51361G>C