Canonical Allele Identifier: CA407462064

Gene: BRSK1

Linked Data

• MyVariant Identifiers: chr19:g.55820070A>G (hg19) ; chr19:g.55308702A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308702A>G , CM000681.2:g.55308702A>G	GRCh38
NC_000019.9:g.55820070A>G , CM000681.1:g.55820070A>G	GRCh37
NC_000019.8:g.60511882A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2153A>G MANE Select	ENSP00000310649.1:p.Asp718Gly
ENST00000309383.5:c.2153A>G	ENSP00000310649.1:p.Asp718Gly
ENST00000326848.7:c.1238A>G	ENSP00000320853.7:p.Asp413Gly
ENST00000590333.5:c.2201A>G	ENSP00000468190.1:p.Asp734Gly
NM_032430.1:c.2153A>G	NP_115806.1:p.Asp718Gly
XM_005259327.2:c.1883A>G	XP_005259384.1:p.Asp628Gly
XM_011527395.1:c.1910A>G	XP_011525697.1:p.Asp637Gly
XR_430213.2:n.2136A>G
XM_005259327.3:c.1883A>G	XP_005259384.1:p.Asp628Gly
XM_011527395.2:c.1625A>G	XP_011525697.2:p.Asp542Gly
XM_024451739.1:c.1928A>G	XP_024307507.1:p.Asp643Gly
XR_430213.4:n.2434A>G
NM_032430.2:c.2153A>G MANE Select	NP_115806.1:p.Asp718Gly