Canonical Allele Identifier: CA348425684

Gene: LIMS2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127642938T>C , CM000664.2:g.127642938T>C	GRCh38
NC_000002.11:g.128400513T>C , CM000664.1:g.128400513T>C	GRCh37
NC_000002.10:g.128116983T>C	NCBI36
NG_042235.1:g.43849A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001161403.3:c.494A>G MANE Select	NP_001154875.1:p.Asn165Ser
ENST00000355119.9:c.494A>G MANE Select	ENSP00000347240.4:p.Asn165Ser
NM_001136037.2:c.560A>G	NP_001129509.2:p.Asn187Ser
NM_001136037.3:c.560A>G	NP_001129509.2:p.Asn187Ser
NM_001136037.4:c.560A>G	NP_001129509.2:p.Asn187Ser
NM_001161403.1:c.494A>G	NP_001154875.1:p.Asn165Ser
NM_001161403.2:c.494A>G	NP_001154875.1:p.Asn165Ser
NM_001161404.1:c.479A>G	NP_001154876.1:p.Asn160Ser
NM_001161404.2:c.479A>G	NP_001154876.1:p.Asn160Ser
NM_001256542.1:c.38A>G	NP_001243471.1:p.Asn13Ser
NM_001256542.2:c.38A>G	NP_001243471.1:p.Asn13Ser
NM_017980.4:c.566A>G	NP_060450.2:p.Asn189Ser
NM_017980.5:c.566A>G	NP_060450.2:p.Asn189Ser
ENST00000324938.9:c.566A>G	ENSP00000326888.5:p.Asn189Ser
ENST00000355119.8:c.494A>G	ENSP00000347240.4:p.Asn165Ser
ENST00000409254.1:c.38A>G	ENSP00000386907.1:p.Asn13Ser
ENST00000409286.5:c.38A>G	ENSP00000386252.1:p.Asn13Ser
ENST00000409455.5:c.479A>G	ENSP00000386383.1:p.Asn160Ser
ENST00000409754.5:c.38A>G	ENSP00000386345.1:p.Asn13Ser
ENST00000409808.6:c.479A>G	ENSP00000386637.2:p.Asn160Ser
ENST00000410011.5:c.479A>G	ENSP00000387002.1:p.Asn160Ser
ENST00000410038.5:c.38A>G	ENSP00000386570.1:p.Asn13Ser
ENST00000413578.5:c.38A>G	ENSP00000388611.1:p.Asn13Ser
ENST00000466410.5:n.630A>G
ENST00000469300.6:n.1512A>G
ENST00000476932.5:n.882A>G
ENST00000545738.6:c.560A>G	ENSP00000443794.2:p.Asn187Ser
ENST00000582671.1:n.441A>G
ENST00000612860.4:c.218A>G	ENSP00000484949.1:p.Asn73Ser
XM_005263709.2:c.479A>G	XP_005263766.1:p.Asn160Ser
XM_005263710.2:c.287A>G	XP_005263767.1:p.Asn96Ser
XM_006712627.2:c.146A>G	XP_006712690.1:p.Asn49Ser
XM_006712627.4:c.146A>G	XP_006712690.1:p.Asn49Ser
XM_011511453.1:c.566A>G	XP_011509755.1:p.Asn189Ser
XM_024452983.1:c.479A>G	XP_024308751.1:p.Asn160Ser
XM_024452984.1:c.479A>G	XP_024308752.1:p.Asn160Ser
XM_024452985.1:c.38A>G	XP_024308753.1:p.Asn13Ser
XM_024452986.1:c.38A>G	XP_024308754.1:p.Asn13Ser
XR_922961.1:n.630A>G
XR_922961.2:n.630A>G