Canonical Allele Identifier: CA1863539181

Gene: SYK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.90870686C= , CM000671.2:g.90870686C=	GRCh38
NC_000009.11:g.93632968C= , CM000671.1:g.93632968C=	GRCh37
NC_000009.10:g.92672789C=	NCBI36
NG_017046.1:g.73957C=
NG_017046.2:g.73957C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375754.9:c.915+3487C= MANE Select	ENSP00000364907.4:n.915+3487C=
ENST00000375746.1:c.915+3487C=	ENSP00000364898.1:n.915+3487C=
ENST00000375747.5:c.847-3518C=	ENSP00000364899.1:n.847-3518C=
ENST00000375751.8:c.847-3518C=	ENSP00000364904.4:n.847-3518C=
ENST00000375754.8:c.915+3487C=	ENSP00000364907.4:n.915+3487C=
NM_001135052.3:c.847-3518C=	NP_001128524.1:n.847-3518C=
NM_001174167.2:c.915+3487C=	NP_001167638.1:n.915+3487C=
NM_001174168.2:c.847-3518C=	NP_001167639.1:n.847-3518C=
NM_003177.6:c.915+3487C=	NP_003168.2:n.915+3487C=
XM_005252147.2:c.915+3487C=	XP_005252204.1:n.915+3487C=
XM_011518946.1:c.915+3487C=	XP_011517248.1:n.915+3487C=
XM_011518947.1:c.847-3518C=	XP_011517249.1:n.847-3518C=
XR_929837.1:n.1118+3450C=
XM_005252147.4:c.915+3487C=	XP_005252204.1:n.915+3487C=
XM_011518946.3:c.915+3487C=	XP_011517248.1:n.915+3487C=
XR_001746370.2:n.1118+3450C=
NM_003177.7:c.915+3487C= MANE Select	NP_003168.2:n.915+3487C=
NM_001135052.4:c.847-3518C=	NP_001128524.1:n.847-3518C=
NM_001174167.3:c.915+3487C=	NP_001167638.1:n.915+3487C=
NM_001174168.3:c.847-3518C=	NP_001167639.1:n.847-3518C=