Canonical Allele Identifier: CA407461974

Gene: BRSK1

Linked Data

• MyVariant Identifiers: chr19:g.55820052A>T (hg19) ; chr19:g.55308684A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308684A>T , CM000681.2:g.55308684A>T	GRCh38
NC_000019.9:g.55820052A>T , CM000681.1:g.55820052A>T	GRCh37
NC_000019.8:g.60511864A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2135A>T MANE Select	ENSP00000310649.1:p.Gln712Leu
ENST00000309383.5:c.2135A>T	ENSP00000310649.1:p.Gln712Leu
ENST00000326848.7:c.1220A>T	ENSP00000320853.7:p.Gln407Leu
ENST00000590333.5:c.2183A>T	ENSP00000468190.1:p.Gln728Leu
NM_032430.1:c.2135A>T	NP_115806.1:p.Gln712Leu
XM_005259327.2:c.1865A>T	XP_005259384.1:p.Gln622Leu
XM_011527395.1:c.1892A>T	XP_011525697.1:p.Gln631Leu
XR_430213.2:n.2118A>T
XM_005259327.3:c.1865A>T	XP_005259384.1:p.Gln622Leu
XM_011527395.2:c.1607A>T	XP_011525697.2:p.Gln536Leu
XM_024451739.1:c.1910A>T	XP_024307507.1:p.Gln637Leu
XR_430213.4:n.2416A>T
NM_032430.2:c.2135A>T MANE Select	NP_115806.1:p.Gln712Leu