Canonical Allele Identifier: CA508995461

Gene: BRSK1

Linked Data

• MyVariant Identifiers: chr19:g.55820023C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308655C>T , CM000681.2:g.55308655C>T	GRCh38
NC_000019.9:g.55820023C>T , CM000681.1:g.55820023C>T	GRCh37
NC_000019.8:g.60511835C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2106C>T MANE Select	ENSP00000310649.1:p.Phe702=
ENST00000309383.5:c.2106C>T	ENSP00000310649.1:p.Phe702=
ENST00000326848.7:c.1191C>T	ENSP00000320853.7:p.Phe397=
ENST00000590333.5:c.2154C>T	ENSP00000468190.1:p.Phe718=
NM_032430.1:c.2106C>T	NP_115806.1:p.Phe702=
XM_005259327.2:c.1836C>T	XP_005259384.1:p.Phe612=
XM_011527395.1:c.1863C>T	XP_011525697.1:p.Phe621=
XR_430213.2:n.2089C>T
XM_005259327.3:c.1836C>T	XP_005259384.1:p.Phe612=
XM_011527395.2:c.1578C>T	XP_011525697.2:p.Phe526=
XM_024451739.1:c.1881C>T	XP_024307507.1:p.Phe627=
XR_430213.4:n.2387C>T
NM_032430.2:c.2106C>T MANE Select	NP_115806.1:p.Phe702=