Canonical Allele Identifier: CA294535712

Gene: SLC39A11

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.72830265G>A , CM000679.2:g.72830265G>A	GRCh38
NC_000017.10:g.70826404G>A , CM000679.1:g.70826404G>A	GRCh37
NC_000017.9:g.68337999G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255559.8:c.601+19369C>T MANE Select	ENSP00000255559.3:n.601+19369C>T
ENST00000255559.7:c.601+19369C>T	ENSP00000255559.3:n.601+19369C>T
ENST00000542342.6:c.622+19369C>T	ENSP00000445829.2:n.622+19369C>T
ENST00000579319.1:c.144-12330C>T
ENST00000579491.1:n.416-6382C>T
ENST00000581581.1:c.73+19369C>T	ENSP00000463083.1:n.73+19369C>T
ENST00000582769.5:c.349+19369C>T	ENSP00000463467.1:n.349+19369C>T
ENST00000583715.5:c.172-8243C>T
ENST00000584129.1:c.*307-6382C>T	ENSP00000464302.1:n.*307-6382C>T
NM_001159770.1:c.622+19369C>T	NP_001153242.1:n.622+19369C>T
NM_139177.3:c.601+19369C>T	NP_631916.2:n.601+19369C>T
XM_005257134.2:c.601+19369C>T	XP_005257191.1:n.601+19369C>T
XM_006721754.2:c.622+19369C>T	XP_006721817.1:n.622+19369C>T
XM_006721755.2:c.622+19369C>T	XP_006721818.1:n.622+19369C>T
XM_006721756.2:c.622+19369C>T	XP_006721819.1:n.622+19369C>T
XM_006721757.2:c.452-93546C>T	XP_006721820.1:n.452-93546C>T
XM_006721758.2:c.623-6382C>T	XP_006721821.1:n.623-6382C>T
XM_006721759.1:c.622+19369C>T	XP_006721822.1:n.622+19369C>T
XM_011524493.1:c.622+19369C>T	XP_011522795.1:n.622+19369C>T
XM_011524494.1:c.622+19369C>T	XP_011522796.1:n.622+19369C>T
XM_011524495.1:c.622+19369C>T	XP_011522797.1:n.622+19369C>T
XM_011524496.1:c.623-11861C>T	XP_011522798.1:n.623-11861C>T
XM_011524498.1:c.623-13879C>T	XP_011522800.1:n.623-13879C>T
XR_429877.2:n.737+19369C>T
NM_001352691.1:c.601+19369C>T	NP_001339620.1:n.601+19369C>T
NM_001352692.1:c.622+19369C>T	NP_001339621.1:n.622+19369C>T
NM_001352693.1:c.601+19369C>T	NP_001339622.1:n.601+19369C>T
XM_006721756.3:c.622+19369C>T	XP_006721819.1:n.622+19369C>T
XM_006721758.4:c.623-6382C>T	XP_006721821.1:n.623-6382C>T
XM_011524494.2:c.622+19369C>T	XP_011522796.1:n.622+19369C>T
XM_011524495.3:c.622+19369C>T	XP_011522797.1:n.622+19369C>T
XM_011524496.2:c.623-11861C>T	XP_011522798.1:n.623-11861C>T
XM_011524498.3:c.623-13879C>T	XP_011522800.1:n.623-13879C>T
XM_017024330.1:c.601+19369C>T	XP_016879819.1:n.601+19369C>T
XM_017024332.1:c.601+19369C>T	XP_016879821.1:n.601+19369C>T
XM_017024333.1:c.472+19369C>T	XP_016879822.1:n.472+19369C>T
XM_017024334.2:c.452-93546C>T	XP_016879823.1:n.452-93546C>T
XM_017024335.1:c.431-93546C>T	XP_016879824.1:n.431-93546C>T
XM_017024336.2:c.472+19369C>T	XP_016879825.1:n.472+19369C>T
XM_017024337.1:c.472+19369C>T	XP_016879826.1:n.472+19369C>T
XM_017024338.1:c.623-8243C>T	XP_016879827.1:n.623-8243C>T
XM_017024339.1:c.602-8243C>T	XP_016879828.1:n.602-8243C>T
XM_017024340.2:c.602-6382C>T	XP_016879829.1:n.602-6382C>T
XM_017024341.2:c.602-6382C>T	XP_016879830.1:n.602-6382C>T
XM_017024342.1:c.601+19369C>T	XP_016879831.1:n.601+19369C>T
NM_001159770.2:c.622+19369C>T	NP_001153242.1:n.622+19369C>T
NM_001352691.2:c.601+19369C>T	NP_001339620.1:n.601+19369C>T
NM_001352692.2:c.622+19369C>T	NP_001339621.1:n.622+19369C>T
NM_001352693.2:c.601+19369C>T	NP_001339622.1:n.601+19369C>T
NM_139177.4:c.601+19369C>T MANE Select	NP_631916.2:n.601+19369C>T