Canonical Allele Identifier: CA12742155

Gene: KHDRBS3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.135472147T>A , CM000670.2:g.135472147T>A	GRCh38
NC_000008.10:g.136484390T>A , CM000670.1:g.136484390T>A	GRCh37
NC_000008.9:g.136553572T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704572.1:c.460+14193T>A	ENSP00000515947.1:n.460+14193T>A
ENST00000355849.10:c.88+14193T>A MANE Select	ENSP00000348108.5:n.88+14193T>A
ENST00000355849.9:c.88+14193T>A	ENSP00000348108.5:n.88+14193T>A
ENST00000517394.5:c.7+13237T>A	ENSP00000430284.1:n.7+13237T>A
ENST00000520981.5:c.7+13237T>A	ENSP00000428607.1:n.7+13237T>A
ENST00000524199.5:c.4+13964T>A	ENSP00000431022.1:n.4+13964T>A
NM_006558.2:c.88+14193T>A	NP_006549.1:n.88+14193T>A
XM_005250757.1:c.4+13964T>A	XP_005250814.1:n.4+13964T>A
XM_005250758.2:c.88+14193T>A	XP_005250815.1:n.88+14193T>A
XM_011516796.1:c.88+8171T>A	XP_011515098.1:n.88+8171T>A
XM_011516797.1:c.7+13237T>A	XP_011515099.1:n.7+13237T>A
XM_011516798.1:c.88+14193T>A	XP_011515100.1:n.88+14193T>A
XM_011516799.1:c.88+14193T>A	XP_011515101.1:n.88+14193T>A
XR_242372.2:n.494+14193T>A
XR_242374.2:n.494+14193T>A
XR_928287.1:n.494+14193T>A
XM_005250757.3:c.4+13964T>A	XP_005250814.1:n.4+13964T>A
XM_005250758.3:c.88+14193T>A	XP_005250815.1:n.88+14193T>A
XM_011516796.3:c.88+8171T>A	XP_011515098.1:n.88+8171T>A
XM_011516797.2:c.7+13237T>A	XP_011515099.1:n.7+13237T>A
XM_024447052.1:c.4+13964T>A	XP_024302820.1:n.4+13964T>A
XR_001745455.1:n.494+14193T>A
XR_001745456.1:n.367+13237T>A
XR_001745457.1:n.237+13964T>A
XR_001745458.1:n.494+14193T>A
XR_242374.3:n.494+14193T>A
NM_006558.3:c.88+14193T>A MANE Select	NP_006549.1:n.88+14193T>A