Canonical Allele Identifier: CA537623573

Gene: STK39

Linked Data

• dbSNP Id: rs1192611384
• gnomAD v2: 2-169041156-C-CG
• gnomAD v3: 2-168184646-C-CG
• gnomAD v4: 2-168184646-C-CG
• MyVariant Identifiers: chr2:g.169041156_169041157insG (hg19) ; chr2:g.168184646_168184647insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168184646_168184647insG , CM000664.2:g.168184646_168184647insG	GRCh38
NC_000002.11:g.169041156_169041157insG , CM000664.1:g.169041156_169041157insG	GRCh37
NC_000002.10:g.168749402_168749403insG	NCBI36
NG_052783.1:g.67949_67950insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697205.1:c.209-2557_209-2556insC	ENSP00000513185.1:n.209-2557_209-2556insC
ENST00000355999.5:c.209-2557_209-2556insC MANE Select	ENSP00000348278.4:n.209-2557_209-2556insC
ENST00000355999.4:c.209-2557_209-2556insC	ENSP00000348278.4:n.209-2557_209-2556insC
NM_013233.2:c.209-2557_209-2556insC	NP_037365.2:n.209-2557_209-2556insC
XM_005246465.2:c.209-2557_209-2556insC	XP_005246522.1:n.209-2557_209-2556insC
XM_011510966.1:c.209-2557_209-2556insC	XP_011509268.1:n.209-2557_209-2556insC
XM_011510967.1:c.209-2557_209-2556insC	XP_011509269.1:n.209-2557_209-2556insC
XM_011510968.1:c.209-2557_209-2556insC	XP_011509270.1:n.209-2557_209-2556insC
XM_017003813.2:c.209-2557_209-2556insC	XP_016859302.1:n.209-2557_209-2556insC
XM_017003814.2:c.209-2557_209-2556insC	XP_016859303.1:n.209-2557_209-2556insC
XM_017003815.2:c.-98-2557_-98-2556insC	XP_016859304.1:n.-98-2557_-98-2556insC
XM_017003816.2:c.209-2557_209-2556insC	XP_016859305.1:n.209-2557_209-2556insC
NM_013233.3:c.209-2557_209-2556insC MANE Select	NP_037365.2:n.209-2557_209-2556insC