Canonical Allele Identifier: CA807583518

Gene: STK10

Linked Data

• dbSNP Id: rs1168892382
• MyVariant Identifiers: chr5:g.171559436C>A (hg19) ; chr5:g.172132432C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.172132432C>A , CM000667.2:g.172132432C>A	GRCh38
NC_000005.9:g.171559436C>A , CM000667.1:g.171559436C>A	GRCh37
NC_000005.8:g.171492041C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000176763.10:c.322-5011G>T MANE Select	ENSP00000176763.5:n.322-5011G>T
ENST00000176763.9:c.322-5011G>T	ENSP00000176763.5:n.322-5011G>T
ENST00000519710.1:n.103-5011G>T
NM_005990.3:c.322-5011G>T	NP_005981.3:n.322-5011G>T
XM_011534641.1:c.322-5011G>T	XP_011532943.1:n.322-5011G>T
XM_011534643.1:c.322-5011G>T	XP_011532945.1:n.322-5011G>T
XM_011534644.1:c.322-5011G>T	XP_011532946.1:n.322-5011G>T
XM_017009788.1:c.-3-5011G>T	XP_016865277.1:n.-3-5011G>T
NM_005990.4:c.322-5011G>T MANE Select	NP_005981.3:n.322-5011G>T