Canonical Allele Identifier: CA14439733
Gene: SLC39A11 HGNC NCBI

Linked Data

dbSNP Id: rs11871756

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72730105C>G , CM000679.2:g.72730105C>G GRCh38
NC_000017.10:g.70726244C>G , CM000679.1:g.70726244C>G GRCh37
NC_000017.9:g.68237839C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000255559.8:c.671+6545G>C MANE Select ENSP00000255559.3:n.671+6545G>C
ENST00000255559.7:c.671+6545G>C ENSP00000255559.3:n.671+6545G>C
ENST00000542342.6:c.692+6545G>C ENSP00000445829.2:n.692+6545G>C
ENST00000579319.1:c.279+6545G>C
ENST00000581581.1:c.143+6545G>C ENSP00000463083.1:n.143+6545G>C
ENST00000582769.5:c.419+6545G>C ENSP00000463467.1:n.419+6545G>C
NM_001159770.1:c.692+6545G>C NP_001153242.1:n.692+6545G>C
NM_139177.3:c.671+6545G>C NP_631916.2:n.671+6545G>C
XM_005257134.2:c.671+6545G>C XP_005257191.1:n.671+6545G>C
XM_006721754.2:c.692+6545G>C XP_006721817.1:n.692+6545G>C
XM_006721755.2:c.692+6545G>C XP_006721818.1:n.692+6545G>C
XM_006721756.2:c.693-4269G>C XP_006721819.1:n.693-4269G>C
XM_006721757.2:c.521+6545G>C XP_006721820.1:n.521+6545G>C
XM_006721759.1:c.692+6545G>C XP_006721822.1:n.692+6545G>C
XM_011524493.1:c.692+6545G>C XP_011522795.1:n.692+6545G>C
XM_011524494.1:c.692+6545G>C XP_011522796.1:n.692+6545G>C
XM_011524495.1:c.692+6545G>C XP_011522797.1:n.692+6545G>C
XR_429877.2:n.808-4269G>C
NM_001352691.1:c.671+6545G>C NP_001339620.1:n.671+6545G>C
NM_001352692.1:c.692+6545G>C NP_001339621.1:n.692+6545G>C
NM_001352693.1:c.671+6545G>C NP_001339622.1:n.671+6545G>C
XM_006721756.3:c.693-4269G>C XP_006721819.1:n.693-4269G>C
XM_011524494.2:c.692+6545G>C XP_011522796.1:n.692+6545G>C
XM_011524495.3:c.692+6545G>C XP_011522797.1:n.692+6545G>C
XM_017024330.1:c.671+6545G>C XP_016879819.1:n.671+6545G>C
XM_017024332.1:c.671+6545G>C XP_016879821.1:n.671+6545G>C
XM_017024333.1:c.542+6545G>C XP_016879822.1:n.542+6545G>C
XM_017024334.2:c.521+6545G>C XP_016879823.1:n.521+6545G>C
XM_017024335.1:c.500+6545G>C XP_016879824.1:n.500+6545G>C
XM_017024336.2:c.542+6545G>C XP_016879825.1:n.542+6545G>C
XM_017024337.1:c.542+6545G>C XP_016879826.1:n.542+6545G>C
XM_017024342.1:c.671+6545G>C XP_016879831.1:n.671+6545G>C
NM_001159770.2:c.692+6545G>C NP_001153242.1:n.692+6545G>C
NM_001352691.2:c.671+6545G>C NP_001339620.1:n.671+6545G>C
NM_001352692.2:c.692+6545G>C NP_001339621.1:n.692+6545G>C
NM_001352693.2:c.671+6545G>C NP_001339622.1:n.671+6545G>C
NM_139177.4:c.671+6545G>C MANE Select NP_631916.2:n.671+6545G>C