Canonical Allele Identifier: CA1826307104

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414344_144414345delinsAC , CM000670.2:g.144414344_144414345delinsAC	GRCh38
NC_000008.10:g.145639728_145639729delinsAC , CM000670.1:g.145639728_145639729delinsAC	GRCh37
NC_000008.9:g.145610536_145610537delinsAC	NCBI36
NG_012234.2:g.7546_7547delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1066_1067delinsGT MANE Select	ENSP00000301305.4:p.Val356=
ENST00000276833.9:c.991_992delinsGT	ENSP00000276833.5:p.Val331=
ENST00000301305.7:c.1066_1067delinsGT	ENSP00000301305.3:p.Val356=
NM_017767.2:c.991_992delinsGT	NP_060237.2:p.Val331=
NM_130849.3:c.1066_1067delinsGT	NP_570901.2:p.Val356=
XM_006716599.1:c.1066_1067delinsGT	XP_006716662.1:p.Val356=
XM_011517153.1:c.784_785delinsGT	XP_011515455.1:p.Val262=
XM_024447188.1:c.784_785delinsGT	XP_024302956.1:p.Val262=
XM_024447189.1:c.784_785delinsGT	XP_024302957.1:p.Val262=
NM_001374839.1:c.784_785delinsGT	NP_001361768.1:p.Val262=
NM_017767.3:c.991_992delinsGT	NP_060237.3:p.Val331=
NM_130849.4:c.1066_1067delinsGT MANE Select	NP_570901.3:p.Val356=