Canonical Allele Identifier: CA407462164

Gene: BRSK1

Linked Data

• gnomAD v4: 19-55308720-C-T
• MyVariant Identifiers: chr19:g.55820088C>T (hg19) ; chr19:g.55308720C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308720C>T , CM000681.2:g.55308720C>T	GRCh38
NC_000019.9:g.55820088C>T , CM000681.1:g.55820088C>T	GRCh37
NC_000019.8:g.60511900C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2171C>T MANE Select	ENSP00000310649.1:p.Ala724Val
ENST00000309383.5:c.2171C>T	ENSP00000310649.1:p.Ala724Val
ENST00000326848.7:c.1256C>T	ENSP00000320853.7:p.Ala419Val
ENST00000590333.5:c.2219C>T	ENSP00000468190.1:p.Ala740Val
NM_032430.1:c.2171C>T	NP_115806.1:p.Ala724Val
XM_005259327.2:c.1901C>T	XP_005259384.1:p.Ala634Val
XM_011527395.1:c.1928C>T	XP_011525697.1:p.Ala643Val
XR_430213.2:n.2154C>T
XM_005259327.3:c.1901C>T	XP_005259384.1:p.Ala634Val
XM_011527395.2:c.1643C>T	XP_011525697.2:p.Ala548Val
XM_024451739.1:c.1946C>T	XP_024307507.1:p.Ala649Val
XR_430213.4:n.2452C>T
NM_032430.2:c.2171C>T MANE Select	NP_115806.1:p.Ala724Val