Canonical Allele Identifier: CA1863526056
Gene: SYK HGNC NCBI

Linked Data

dbSNP Id: rs1828822757

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.90892286C>A , CM000671.2:g.90892286C>A GRCh38
NC_000009.11:g.93654568C>A , CM000671.1:g.93654568C>A GRCh37
NC_000009.10:g.92694389C>A NCBI36
NG_017046.1:g.95557C>A
NG_017046.2:g.95557C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375754.9:c.1836-3242C>A MANE Select ENSP00000364907.4:n.1836-3242C>A
ENST00000375746.1:c.1836-3242C>A ENSP00000364898.1:n.1836-3242C>A
ENST00000375747.5:c.1767-3242C>A ENSP00000364899.1:n.1767-3242C>A
ENST00000375751.8:c.1767-3242C>A ENSP00000364904.4:n.1767-3242C>A
ENST00000375754.8:c.1836-3242C>A ENSP00000364907.4:n.1836-3242C>A
NM_001135052.3:c.1767-3242C>A NP_001128524.1:n.1767-3242C>A
NM_001174167.2:c.1836-3242C>A NP_001167638.1:n.1836-3242C>A
NM_001174168.2:c.1767-3242C>A NP_001167639.1:n.1767-3242C>A
NM_003177.6:c.1836-3242C>A NP_003168.2:n.1836-3242C>A
XM_005252147.2:c.1836-3242C>A XP_005252204.1:n.1836-3242C>A
XM_011518946.1:c.1836-3242C>A XP_011517248.1:n.1836-3242C>A
XM_011518947.1:c.1767-3242C>A XP_011517249.1:n.1767-3242C>A
XM_005252147.4:c.1836-3242C>A XP_005252204.1:n.1836-3242C>A
XM_011518946.3:c.1836-3242C>A XP_011517248.1:n.1836-3242C>A
XR_001746370.2:n.2039-3242C>A
NM_003177.7:c.1836-3242C>A MANE Select NP_003168.2:n.1836-3242C>A
NM_001135052.4:c.1767-3242C>A NP_001128524.1:n.1767-3242C>A
NM_001174167.3:c.1836-3242C>A NP_001167638.1:n.1836-3242C>A
NM_001174168.3:c.1767-3242C>A NP_001167639.1:n.1767-3242C>A