Canonical Allele Identifier: CA508995520

Gene: BRSK1

Linked Data

• MyVariant Identifiers: chr19:g.55820065T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308697T>A , CM000681.2:g.55308697T>A	GRCh38
NC_000019.9:g.55820065T>A , CM000681.1:g.55820065T>A	GRCh37
NC_000019.8:g.60511877T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2148T>A MANE Select	ENSP00000310649.1:p.Thr716=
ENST00000309383.5:c.2148T>A	ENSP00000310649.1:p.Thr716=
ENST00000326848.7:c.1233T>A	ENSP00000320853.7:p.Thr411=
ENST00000590333.5:c.2196T>A	ENSP00000468190.1:p.Thr732=
NM_032430.1:c.2148T>A	NP_115806.1:p.Thr716=
XM_005259327.2:c.1878T>A	XP_005259384.1:p.Thr626=
XM_011527395.1:c.1905T>A	XP_011525697.1:p.Thr635=
XR_430213.2:n.2131T>A
XM_005259327.3:c.1878T>A	XP_005259384.1:p.Thr626=
XM_011527395.2:c.1620T>A	XP_011525697.2:p.Thr540=
XM_024451739.1:c.1923T>A	XP_024307507.1:p.Thr641=
XR_430213.4:n.2429T>A
NM_032430.2:c.2148T>A MANE Select	NP_115806.1:p.Thr716=