Canonical Allele Identifier: CA407462001

Gene: BRSK1

Linked Data

• MyVariant Identifiers: chr19:g.55820060A>C (hg19) ; chr19:g.55308692A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308692A>C , CM000681.2:g.55308692A>C	GRCh38
NC_000019.9:g.55820060A>C , CM000681.1:g.55820060A>C	GRCh37
NC_000019.8:g.60511872A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2143A>C MANE Select	ENSP00000310649.1:p.Ser715Arg
ENST00000309383.5:c.2143A>C	ENSP00000310649.1:p.Ser715Arg
ENST00000326848.7:c.1228A>C	ENSP00000320853.7:p.Ser410Arg
ENST00000590333.5:c.2191A>C	ENSP00000468190.1:p.Ser731Arg
NM_032430.1:c.2143A>C	NP_115806.1:p.Ser715Arg
XM_005259327.2:c.1873A>C	XP_005259384.1:p.Ser625Arg
XM_011527395.1:c.1900A>C	XP_011525697.1:p.Ser634Arg
XR_430213.2:n.2126A>C
XM_005259327.3:c.1873A>C	XP_005259384.1:p.Ser625Arg
XM_011527395.2:c.1615A>C	XP_011525697.2:p.Ser539Arg
XM_024451739.1:c.1918A>C	XP_024307507.1:p.Ser640Arg
XR_430213.4:n.2424A>C
NM_032430.2:c.2143A>C MANE Select	NP_115806.1:p.Ser715Arg