Canonical Allele Identifier: CA1863526085
Gene: SYK HGNC NCBI

Linked Data

dbSNP Id: rs1587930444

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.90892339A>G , CM000671.2:g.90892339A>G GRCh38
NC_000009.11:g.93654621A>G , CM000671.1:g.93654621A>G GRCh37
NC_000009.10:g.92694442A>G NCBI36
NG_017046.1:g.95610A>G
NG_017046.2:g.95610A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375754.9:c.1836-3189A>G MANE Select ENSP00000364907.4:n.1836-3189A>G
ENST00000375746.1:c.1836-3189A>G ENSP00000364898.1:n.1836-3189A>G
ENST00000375747.5:c.1767-3189A>G ENSP00000364899.1:n.1767-3189A>G
ENST00000375751.8:c.1767-3189A>G ENSP00000364904.4:n.1767-3189A>G
ENST00000375754.8:c.1836-3189A>G ENSP00000364907.4:n.1836-3189A>G
NM_001135052.3:c.1767-3189A>G NP_001128524.1:n.1767-3189A>G
NM_001174167.2:c.1836-3189A>G NP_001167638.1:n.1836-3189A>G
NM_001174168.2:c.1767-3189A>G NP_001167639.1:n.1767-3189A>G
NM_003177.6:c.1836-3189A>G NP_003168.2:n.1836-3189A>G
XM_005252147.2:c.1836-3189A>G XP_005252204.1:n.1836-3189A>G
XM_011518946.1:c.1836-3189A>G XP_011517248.1:n.1836-3189A>G
XM_011518947.1:c.1767-3189A>G XP_011517249.1:n.1767-3189A>G
XM_005252147.4:c.1836-3189A>G XP_005252204.1:n.1836-3189A>G
XM_011518946.3:c.1836-3189A>G XP_011517248.1:n.1836-3189A>G
XR_001746370.2:n.2039-3189A>G
NM_003177.7:c.1836-3189A>G MANE Select NP_003168.2:n.1836-3189A>G
NM_001135052.4:c.1767-3189A>G NP_001128524.1:n.1767-3189A>G
NM_001174167.3:c.1836-3189A>G NP_001167638.1:n.1836-3189A>G
NM_001174168.3:c.1767-3189A>G NP_001167639.1:n.1767-3189A>G