Canonical Allele Identifier: CA564647075

Gene: STK10

Linked Data

• dbSNP Id: rs1389449111
• gnomAD v2: 5-171559392-A-G
• gnomAD v3: 5-172132388-A-G
• gnomAD v4: 5-172132388-A-G
• MyVariant Identifiers: chr5:g.171559392A>G (hg19) ; chr5:g.172132388A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.172132388A>G , CM000667.2:g.172132388A>G	GRCh38
NC_000005.9:g.171559392A>G , CM000667.1:g.171559392A>G	GRCh37
NC_000005.8:g.171491997A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176763.10:c.322-4967T>C MANE Select	ENSP00000176763.5:n.322-4967T>C
ENST00000176763.9:c.322-4967T>C	ENSP00000176763.5:n.322-4967T>C
ENST00000519710.1:n.103-4967T>C
NM_005990.3:c.322-4967T>C	NP_005981.3:n.322-4967T>C
XM_011534641.1:c.322-4967T>C	XP_011532943.1:n.322-4967T>C
XM_011534643.1:c.322-4967T>C	XP_011532945.1:n.322-4967T>C
XM_011534644.1:c.322-4967T>C	XP_011532946.1:n.322-4967T>C
XM_017009788.1:c.-3-4967T>C	XP_016865277.1:n.-3-4967T>C
NM_005990.4:c.322-4967T>C MANE Select	NP_005981.3:n.322-4967T>C