Canonical Allele Identifier: CA848876266

Gene: SLC39A4

Linked Data

• dbSNP Id: rs1184115777
• MyVariant Identifiers: chr8:g.144414301_144414302insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414304dup , CM000670.2:g.144414304dup	GRCh38
NC_000008.10:g.145639688dup , CM000670.1:g.145639688dup	GRCh37
NC_000008.9:g.145610496dup	NCBI36
NG_012234.2:g.7589dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1109dup MANE Select	ENSP00000301305.4:p.Ala371CysfsTer?
ENST00000276833.9:c.1034dup	ENSP00000276833.5:p.Ala346CysfsTer?
ENST00000301305.7:c.1109dup	ENSP00000301305.3:p.Ala371CysfsTer?
NM_017767.2:c.1034dup	NP_060237.2:p.Ala346CysfsTer?
NM_130849.3:c.1109dup	NP_570901.2:p.Ala371CysfsTer?
XM_006716599.1:c.1109dup	XP_006716662.1:p.Ala371CysfsTer?
XM_011517153.1:c.827dup	XP_011515455.1:p.Ala277CysfsTer?
XM_024447188.1:c.827dup	XP_024302956.1:p.Ala277CysfsTer?
XM_024447189.1:c.827dup	XP_024302957.1:p.Ala277CysfsTer?
NM_001374839.1:c.827dup	NP_001361768.1:p.Ala277CysfsTer?
NM_017767.3:c.1034dup	NP_060237.3:p.Ala346CysfsTer?
NM_130849.4:c.1109dup MANE Select	NP_570901.3:p.Ala371CysfsTer?