Canonical Allele Identifier: CA407461802

Gene: BRSK1

Linked Data

• MyVariant Identifiers: chr19:g.55820021T>G (hg19) ; chr19:g.55308653T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308653T>G , CM000681.2:g.55308653T>G	GRCh38
NC_000019.9:g.55820021T>G , CM000681.1:g.55820021T>G	GRCh37
NC_000019.8:g.60511833T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2104T>G MANE Select	ENSP00000310649.1:p.Phe702Val
ENST00000309383.5:c.2104T>G	ENSP00000310649.1:p.Phe702Val
ENST00000326848.7:c.1189T>G	ENSP00000320853.7:p.Phe397Val
ENST00000590333.5:c.2152T>G	ENSP00000468190.1:p.Phe718Val
NM_032430.1:c.2104T>G	NP_115806.1:p.Phe702Val
XM_005259327.2:c.1834T>G	XP_005259384.1:p.Phe612Val
XM_011527395.1:c.1861T>G	XP_011525697.1:p.Phe621Val
XR_430213.2:n.2087T>G
XM_005259327.3:c.1834T>G	XP_005259384.1:p.Phe612Val
XM_011527395.2:c.1576T>G	XP_011525697.2:p.Phe526Val
XM_024451739.1:c.1879T>G	XP_024307507.1:p.Phe627Val
XR_430213.4:n.2385T>G
NM_032430.2:c.2104T>G MANE Select	NP_115806.1:p.Phe702Val