Canonical Allele Identifier: CA407462039

Gene: BRSK1

Linked Data

• MyVariant Identifiers: chr19:g.55820064C>G (hg19) ; chr19:g.55308696C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308696C>G , CM000681.2:g.55308696C>G	GRCh38
NC_000019.9:g.55820064C>G , CM000681.1:g.55820064C>G	GRCh37
NC_000019.8:g.60511876C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2147C>G MANE Select	ENSP00000310649.1:p.Thr716Ser
ENST00000309383.5:c.2147C>G	ENSP00000310649.1:p.Thr716Ser
ENST00000326848.7:c.1232C>G	ENSP00000320853.7:p.Thr411Ser
ENST00000590333.5:c.2195C>G	ENSP00000468190.1:p.Thr732Ser
NM_032430.1:c.2147C>G	NP_115806.1:p.Thr716Ser
XM_005259327.2:c.1877C>G	XP_005259384.1:p.Thr626Ser
XM_011527395.1:c.1904C>G	XP_011525697.1:p.Thr635Ser
XR_430213.2:n.2130C>G
XM_005259327.3:c.1877C>G	XP_005259384.1:p.Thr626Ser
XM_011527395.2:c.1619C>G	XP_011525697.2:p.Thr540Ser
XM_024451739.1:c.1922C>G	XP_024307507.1:p.Thr641Ser
XR_430213.4:n.2428C>G
NM_032430.2:c.2147C>G MANE Select	NP_115806.1:p.Thr716Ser