Canonical Allele Identifier: CA2512985975

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414376_144414377insGCCAGGCTCAGGAAGGTCTGCAGGATGTAGTGGGCGACCCCCCTGCAGCCAGTGCAGGTCAGCAGCAGG , CM000670.2:g.144414376_144414377insGCCAGGCTCAGGAAGGTCTGCAGGATGTAGTGGGCGACCCCCCTGCAGCCAGTGCAGGTCAGCAGCAGG	GRCh38
NC_000008.10:g.145639760_145639761insGCCAGGCTCAGGAAGGTCTGCAGGATGTAGTGGGCGACCCCCCTGCAGCCAGTGCAGGTCAGCAGCAGG , CM000670.1:g.145639760_145639761insGCCAGGCTCAGGAAGGTCTGCAGGATGTAGTGGGCGACCCCCCTGCAGCCAGTGCAGGTCAGCAGCAGG	GRCh37
NC_000008.9:g.145610568_145610569insGCCAGGCTCAGGAAGGTCTGCAGGATGTAGTGGGCGACCCCCCTGCAGCCAGTGCAGGTCAGCAGCAGG	NCBI36
NG_012234.2:g.7548_7549insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1068_1069insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC MANE Select	ENSP00000301305.4:p.Val356_Thr357insAlaHisTyrIleLeuGlnThrPheL...
ENST00000276833.9:c.993_994insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC	ENSP00000276833.5:p.Val331_Thr332insAlaHisTyrIleLeuGlnThrPheL...
ENST00000301305.7:c.1068_1069insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC	ENSP00000301305.3:p.Val356_Thr357insAlaHisTyrIleLeuGlnThrPheL...
NM_017767.2:c.993_994insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC	NP_060237.2:p.Val331_Thr332insAlaHisTyrIleLeuGlnThrPheLeuSerL...
NM_130849.3:c.1068_1069insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC	NP_570901.2:p.Val356_Thr357insAlaHisTyrIleLeuGlnThrPheLeuSerL...
XM_006716599.1:c.1068_1069insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC	XP_006716662.1:p.Val356_Thr357insAlaHisTyrIleLeuGlnThrPheLeuS...
XM_011517153.1:c.786_787insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC	XP_011515455.1:p.Val262_Thr263insAlaHisTyrIleLeuGlnThrPheLeuS...
XM_024447188.1:c.786_787insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC	XP_024302956.1:p.Val262_Thr263insAlaHisTyrIleLeuGlnThrPheLeuS...
XM_024447189.1:c.786_787insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC	XP_024302957.1:p.Val262_Thr263insAlaHisTyrIleLeuGlnThrPheLeuS...
NM_001374839.1:c.786_787insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC	NP_001361768.1:p.Val262_Thr263insAlaHisTyrIleLeuGlnThrPheLeuS...
NM_017767.3:c.993_994insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC	NP_060237.3:p.Val331_Thr332insAlaHisTyrIleLeuGlnThrPheLeuSerL...
NM_130849.4:c.1068_1069insGCCCACTACATCCTGCAGACCTTCCTGAGCCTGGCCCTGCTGCTGACCTGCACTGGCTGCAGGGGGGTC MANE Select	NP_570901.3:p.Val356_Thr357insAlaHisTyrIleLeuGlnThrPheLeuSerL...