Canonical Allele Identifier: CA60446146

Gene: STK39

Linked Data

• dbSNP Id: rs1038023759
• gnomAD v2: 2-168811510-C-A
• gnomAD v3: 2-167955000-C-A
• gnomAD v4: 2-167955000-C-A
• MyVariant Identifiers: chr2:g.168811510C>A (hg19) ; chr2:g.167955000C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.167955000C>A , CM000664.2:g.167955000C>A	GRCh38
NC_000002.11:g.168811510C>A , CM000664.1:g.168811510C>A	GRCh37
NC_000002.10:g.168519756C>A	NCBI36
NG_052783.1:g.297596G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697205.1:c.2071G>T	ENSP00000513185.1:n.2071G>T
ENST00000355999.5:c.*496G>T MANE Select	ENSP00000348278.4:n.*496G>T
ENST00000355999.4:c.*496G>T	ENSP00000348278.4:n.*496G>T
ENST00000487143.5:n.1234G>T
NM_013233.2:c.*496G>T	NP_037365.2:n.*496G>T
XM_005246465.2:c.*496G>T	XP_005246522.1:n.*496G>T
XM_011510966.1:c.*496G>T	XP_011509268.1:n.*496G>T
XM_011510967.1:c.*496G>T	XP_011509269.1:n.*496G>T
XM_017003815.2:c.*496G>T	XP_016859304.1:n.*496G>T
XM_017003817.2:c.*496G>T	XP_016859306.1:n.*496G>T
NM_013233.3:c.*496G>T MANE Select	NP_037365.2:n.*496G>T