Canonical Allele Identifier: CA1826307198

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414483_144414497delinsCCTGCTTCCCGGGCG , CM000670.2:g.144414483_144414497delinsCCTGCTTCCCGGGCG	GRCh38
NC_000008.10:g.145639867_145639881delinsCCTGCTTCCCGGGCG , CM000670.1:g.145639867_145639881delinsCCTGCTTCCCGGGCG	GRCh37
NC_000008.9:g.145610675_145610689delinsCCTGCTTCCCGGGCG	NCBI36
NG_012234.2:g.7394_7408delinsCGCCCGGGAAGCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.977-63_977-49delinsCGCCCGGGAAGCAGG MANE Select	ENSP00000301305.4:n.977-63_977-49delinsCGCCCGGGAAGCAGG
ENST00000276833.9:c.902-63_902-49delinsCGCCCGGGAAGCAGG	ENSP00000276833.5:n.902-63_902-49delinsCGCCCGGGAAGCAGG
ENST00000301305.7:c.977-63_977-49delinsCGCCCGGGAAGCAGG	ENSP00000301305.3:n.977-63_977-49delinsCGCCCGGGAAGCAGG
NM_017767.2:c.902-63_902-49delinsCGCCCGGGAAGCAGG	NP_060237.2:n.902-63_902-49delinsCGCCCGGGAAGCAGG
NM_130849.3:c.977-63_977-49delinsCGCCCGGGAAGCAGG	NP_570901.2:n.977-63_977-49delinsCGCCCGGGAAGCAGG
XM_006716599.1:c.977-63_977-49delinsCGCCCGGGAAGCAGG	XP_006716662.1:n.977-63_977-49delinsCGCCCGGGAAGCAGG
XM_011517153.1:c.695-63_695-49delinsCGCCCGGGAAGCAGG	XP_011515455.1:n.695-63_695-49delinsCGCCCGGGAAGCAGG
XM_024447188.1:c.695-63_695-49delinsCGCCCGGGAAGCAGG	XP_024302956.1:n.695-63_695-49delinsCGCCCGGGAAGCAGG
XM_024447189.1:c.695-63_695-49delinsCGCCCGGGAAGCAGG	XP_024302957.1:n.695-63_695-49delinsCGCCCGGGAAGCAGG
NM_001374839.1:c.695-63_695-49delinsCGCCCGGGAAGCAGG	NP_001361768.1:n.695-63_695-49delinsCGCCCGGGAAGCAGG
NM_017767.3:c.902-63_902-49delinsCGCCCGGGAAGCAGG	NP_060237.3:n.902-63_902-49delinsCGCCCGGGAAGCAGG
NM_130849.4:c.977-63_977-49delinsCGCCCGGGAAGCAGG MANE Select	NP_570901.3:n.977-63_977-49delinsCGCCCGGGAAGCAGG