Canonical Allele Identifier: CA2695210375

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414057dup , CM000670.2:g.144414057dup	GRCh38
NC_000008.10:g.145639441dup , CM000670.1:g.145639441dup	GRCh37
NC_000008.9:g.145610249dup	NCBI36
NG_012234.2:g.7836dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1190dup MANE Select	ENSP00000301305.4:p.Gln398ThrfsTer20
ENST00000276833.9:c.1115dup	ENSP00000276833.5:p.Gln373ThrfsTer20
ENST00000301305.7:c.1190dup	ENSP00000301305.3:p.Gln398ThrfsTer20
ENST00000531789.1:n.27dup
NM_017767.2:c.1115dup	NP_060237.2:p.Gln373ThrfsTer20
NM_130849.3:c.1190dup	NP_570901.2:p.Gln398ThrfsTer20
XM_006716599.1:c.1190dup	XP_006716662.1:p.Gln398ThrfsTer20
XM_011517153.1:c.908dup	XP_011515455.1:p.Gln304ThrfsTer20
XM_024447188.1:c.908dup	XP_024302956.1:p.Gln304ThrfsTer20
XM_024447189.1:c.908dup	XP_024302957.1:p.Gln304ThrfsTer20
NM_001374839.1:c.908dup	NP_001361768.1:p.Gln304ThrfsTer20
NM_017767.3:c.1115dup	NP_060237.3:p.Gln373ThrfsTer20
NM_130849.4:c.1190dup MANE Select	NP_570901.3:p.Gln398ThrfsTer20