Canonical Allele Identifier: CA15387348
Gene: STK32A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.147354035C>A , CM000667.2:g.147354035C>A GRCh38
NC_000005.9:g.146733598C>A , CM000667.1:g.146733598C>A GRCh37
NC_000005.8:g.146713791C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397936.8:c.562+2881C>A MANE Select ENSP00000381030.3:n.562+2881C>A
ENST00000648628.1:c.556+2881C>A ENSP00000497167.1:n.556+2881C>A
ENST00000306304.10:n.895+2881C>A
ENST00000397936.7:c.562+2881C>A ENSP00000381030.3:n.562+2881C>A
ENST00000398523.3:c.562+2881C>A ENSP00000381535.3:n.562+2881C>A
NM_001112724.1:c.562+2881C>A NP_001106195.1:n.562+2881C>A
NM_001287740.1:c.562+2881C>A NP_001274669.1:n.562+2881C>A
XM_011537576.1:c.556+2881C>A XP_011535878.1:n.556+2881C>A
XM_011537577.1:c.562+2881C>A XP_011535879.1:n.562+2881C>A
XM_011537578.1:c.562+2881C>A XP_011535880.1:n.562+2881C>A
XM_011537579.1:c.562+2881C>A XP_011535881.1:n.562+2881C>A
XM_011537577.2:c.562+2881C>A XP_011535879.1:n.562+2881C>A
XM_011537579.2:c.562+2881C>A XP_011535881.1:n.562+2881C>A
XM_017009213.1:c.562+2881C>A XP_016864702.1:n.562+2881C>A
XM_017009214.1:c.55+2881C>A XP_016864703.1:n.55+2881C>A
XR_001742037.1:n.895+2881C>A
XR_001742038.1:n.895+2881C>A
NM_001112724.2:c.562+2881C>A MANE Select NP_001106195.1:n.562+2881C>A
NM_001287740.2:c.562+2881C>A NP_001274669.1:n.562+2881C>A
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