Canonical Allele Identifier: CA1826306997

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414189_144414204delinsCCCTGGGAGGGCACGG , CM000670.2:g.144414189_144414204delinsCCCTGGGAGGGCACGG	GRCh38
NG_012234.2:g.7687_7702delinsCCGTGCCCTCCCAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1149+58_1149+73delinsCCGTGCCCTCCCAGGG MANE Select	ENSP00000301305.4:n.1149+58_1149+73delinsCCGTGCCCTCCCAGGG
ENST00000276833.9:c.1074+58_1074+73delinsCCGTGCCCTCCCAGGG	ENSP00000276833.5:n.1074+58_1074+73delinsCCGTGCCCTCCCAGGG
ENST00000301305.7:c.1149+58_1149+73delinsCCGTGCCCTCCCAGGG	ENSP00000301305.3:n.1149+58_1149+73delinsCCGTGCCCTCCCAGGG
NM_017767.2:c.1074+58_1074+73delinsCCGTGCCCTCCCAGGG	NP_060237.2:n.1074+58_1074+73delinsCCGTGCCCTCCCAGGG
NM_130849.3:c.1149+58_1149+73delinsCCGTGCCCTCCCAGGG	NP_570901.2:n.1149+58_1149+73delinsCCGTGCCCTCCCAGGG
XM_006716599.1:c.1149+58_1149+73delinsCCGTGCCCTCCCAGGG	XP_006716662.1:n.1149+58_1149+73delinsCCGTGCCCTCCCAGGG
XM_011517153.1:c.867+58_867+73delinsCCGTGCCCTCCCAGGG	XP_011515455.1:n.867+58_867+73delinsCCGTGCCCTCCCAGGG
XM_024447188.1:c.867+58_867+73delinsCCGTGCCCTCCCAGGG	XP_024302956.1:n.867+58_867+73delinsCCGTGCCCTCCCAGGG
XM_024447189.1:c.867+58_867+73delinsCCGTGCCCTCCCAGGG	XP_024302957.1:n.867+58_867+73delinsCCGTGCCCTCCCAGGG
NM_001374839.1:c.867+58_867+73delinsCCGTGCCCTCCCAGGG	NP_001361768.1:n.867+58_867+73delinsCCGTGCCCTCCCAGGG
NM_017767.3:c.1074+58_1074+73delinsCCGTGCCCTCCCAGGG	NP_060237.3:n.1074+58_1074+73delinsCCGTGCCCTCCCAGGG
NM_130849.4:c.1149+58_1149+73delinsCCGTGCCCTCCCAGGG MANE Select	NP_570901.3:n.1149+58_1149+73delinsCCGTGCCCTCCCAGGG