Canonical Allele Identifier: CA407461862

Gene: BRSK1

Linked Data

• MyVariant Identifiers: chr19:g.55820031T>C (hg19) ; chr19:g.55308663T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308663T>C , CM000681.2:g.55308663T>C	GRCh38
NC_000019.9:g.55820031T>C , CM000681.1:g.55820031T>C	GRCh37
NC_000019.8:g.60511843T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2114T>C MANE Select	ENSP00000310649.1:p.Val705Ala
ENST00000309383.5:c.2114T>C	ENSP00000310649.1:p.Val705Ala
ENST00000326848.7:c.1199T>C	ENSP00000320853.7:p.Val400Ala
ENST00000590333.5:c.2162T>C	ENSP00000468190.1:p.Val721Ala
NM_032430.1:c.2114T>C	NP_115806.1:p.Val705Ala
XM_005259327.2:c.1844T>C	XP_005259384.1:p.Val615Ala
XM_011527395.1:c.1871T>C	XP_011525697.1:p.Val624Ala
XR_430213.2:n.2097T>C
XM_005259327.3:c.1844T>C	XP_005259384.1:p.Val615Ala
XM_011527395.2:c.1586T>C	XP_011525697.2:p.Val529Ala
XM_024451739.1:c.1889T>C	XP_024307507.1:p.Val630Ala
XR_430213.4:n.2395T>C
NM_032430.2:c.2114T>C MANE Select	NP_115806.1:p.Val705Ala