Canonical Allele Identifier: CA407462186

Gene: BRSK1

Linked Data

• MyVariant Identifiers: chr19:g.55820094C>G (hg19) ; chr19:g.55308726C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308726C>G , CM000681.2:g.55308726C>G	GRCh38
NC_000019.9:g.55820094C>G , CM000681.1:g.55820094C>G	GRCh37
NC_000019.8:g.60511906C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2177C>G MANE Select	ENSP00000310649.1:p.Ala726Gly
ENST00000309383.5:c.2177C>G	ENSP00000310649.1:p.Ala726Gly
ENST00000326848.7:c.1262C>G	ENSP00000320853.7:p.Ala421Gly
ENST00000590333.5:c.2225C>G	ENSP00000468190.1:p.Ala742Gly
NM_032430.1:c.2177C>G	NP_115806.1:p.Ala726Gly
XM_005259327.2:c.1907C>G	XP_005259384.1:p.Ala636Gly
XM_011527395.1:c.1934C>G	XP_011525697.1:p.Ala645Gly
XR_430213.2:n.2160C>G
XM_005259327.3:c.1907C>G	XP_005259384.1:p.Ala636Gly
XM_011527395.2:c.1649C>G	XP_011525697.2:p.Ala550Gly
XM_024451739.1:c.1952C>G	XP_024307507.1:p.Ala651Gly
XR_430213.4:n.2458C>G
NM_032430.2:c.2177C>G MANE Select	NP_115806.1:p.Ala726Gly