Canonical Allele Identifier: CA407462144

Gene: BRSK1

Linked Data

• MyVariant Identifiers: chr19:g.55820084C>G (hg19) ; chr19:g.55308716C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308716C>G , CM000681.2:g.55308716C>G	GRCh38
NC_000019.9:g.55820084C>G , CM000681.1:g.55820084C>G	GRCh37
NC_000019.8:g.60511896C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2167C>G MANE Select	ENSP00000310649.1:p.Gln723Glu
ENST00000309383.5:c.2167C>G	ENSP00000310649.1:p.Gln723Glu
ENST00000326848.7:c.1252C>G	ENSP00000320853.7:p.Gln418Glu
ENST00000590333.5:c.2215C>G	ENSP00000468190.1:p.Gln739Glu
NM_032430.1:c.2167C>G	NP_115806.1:p.Gln723Glu
XM_005259327.2:c.1897C>G	XP_005259384.1:p.Gln633Glu
XM_011527395.1:c.1924C>G	XP_011525697.1:p.Gln642Glu
XR_430213.2:n.2150C>G
XM_005259327.3:c.1897C>G	XP_005259384.1:p.Gln633Glu
XM_011527395.2:c.1639C>G	XP_011525697.2:p.Gln547Glu
XM_024451739.1:c.1942C>G	XP_024307507.1:p.Gln648Glu
XR_430213.4:n.2448C>G
NM_032430.2:c.2167C>G MANE Select	NP_115806.1:p.Gln723Glu