Canonical Allele Identifier: CA1826307153

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414417_144414422delinsGGGAGC , CM000670.2:g.144414417_144414422delinsGGGAGC	GRCh38
NC_000008.10:g.145639801_145639806delinsGGGAGC , CM000670.1:g.145639801_145639806delinsGGGAGC	GRCh37
NC_000008.9:g.145610609_145610614delinsGGGAGC	NCBI36
NG_012234.2:g.7469_7474delinsGCTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.989_994delinsGCTCCC MANE Select	ENSP00000301305.4:p.Gly330=
ENST00000276833.9:c.914_919delinsGCTCCC	ENSP00000276833.5:p.Gly305=
ENST00000301305.7:c.989_994delinsGCTCCC	ENSP00000301305.3:p.Gly330=
NM_017767.2:c.914_919delinsGCTCCC	NP_060237.2:p.Gly305=
NM_130849.3:c.989_994delinsGCTCCC	NP_570901.2:p.Gly330=
XM_006716599.1:c.989_994delinsGCTCCC	XP_006716662.1:p.Gly330=
XM_011517153.1:c.707_712delinsGCTCCC	XP_011515455.1:p.Gly236=
XM_024447188.1:c.707_712delinsGCTCCC	XP_024302956.1:p.Gly236=
XM_024447189.1:c.707_712delinsGCTCCC	XP_024302957.1:p.Gly236=
NM_001374839.1:c.707_712delinsGCTCCC	NP_001361768.1:p.Gly236=
NM_017767.3:c.914_919delinsGCTCCC	NP_060237.3:p.Gly305=
NM_130849.4:c.989_994delinsGCTCCC MANE Select	NP_570901.3:p.Gly330=