Canonical Allele Identifier: CA1863526218

Gene: SYK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.90892691_90892692delinsTG , CM000671.2:g.90892691_90892692delinsTG	GRCh38
NC_000009.11:g.93654973_93654974delinsTG , CM000671.1:g.93654973_93654974delinsTG	GRCh37
NC_000009.10:g.92694794_92694795delinsTG	NCBI36
NG_017046.1:g.95962_95963delinsTG
NG_017046.2:g.95962_95963delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375754.9:c.1836-2837_1836-2836delinsTG MANE Select	ENSP00000364907.4:n.1836-2837_1836-2836delinsTG
ENST00000375746.1:c.1836-2837_1836-2836delinsTG	ENSP00000364898.1:n.1836-2837_1836-2836delinsTG
ENST00000375747.5:c.1767-2837_1767-2836delinsTG	ENSP00000364899.1:n.1767-2837_1767-2836delinsTG
ENST00000375751.8:c.1767-2837_1767-2836delinsTG	ENSP00000364904.4:n.1767-2837_1767-2836delinsTG
ENST00000375754.8:c.1836-2837_1836-2836delinsTG	ENSP00000364907.4:n.1836-2837_1836-2836delinsTG
NM_001135052.3:c.1767-2837_1767-2836delinsTG	NP_001128524.1:n.1767-2837_1767-2836delinsTG
NM_001174167.2:c.1836-2837_1836-2836delinsTG	NP_001167638.1:n.1836-2837_1836-2836delinsTG
NM_001174168.2:c.1767-2837_1767-2836delinsTG	NP_001167639.1:n.1767-2837_1767-2836delinsTG
NM_003177.6:c.1836-2837_1836-2836delinsTG	NP_003168.2:n.1836-2837_1836-2836delinsTG
XM_005252147.2:c.1836-2837_1836-2836delinsTG	XP_005252204.1:n.1836-2837_1836-2836delinsTG
XM_011518946.1:c.1836-2837_1836-2836delinsTG	XP_011517248.1:n.1836-2837_1836-2836delinsTG
XM_011518947.1:c.1767-2837_1767-2836delinsTG	XP_011517249.1:n.1767-2837_1767-2836delinsTG
XM_005252147.4:c.1836-2837_1836-2836delinsTG	XP_005252204.1:n.1836-2837_1836-2836delinsTG
XM_011518946.3:c.1836-2837_1836-2836delinsTG	XP_011517248.1:n.1836-2837_1836-2836delinsTG
XR_001746370.2:n.2039-2837_2039-2836delinsTG
NM_003177.7:c.1836-2837_1836-2836delinsTG MANE Select	NP_003168.2:n.1836-2837_1836-2836delinsTG
NM_001135052.4:c.1767-2837_1767-2836delinsTG	NP_001128524.1:n.1767-2837_1767-2836delinsTG
NM_001174167.3:c.1836-2837_1836-2836delinsTG	NP_001167638.1:n.1836-2837_1836-2836delinsTG
NM_001174168.3:c.1767-2837_1767-2836delinsTG	NP_001167639.1:n.1767-2837_1767-2836delinsTG