Canonical Allele Identifier: CA463556155

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414048-G-T
• MyVariant Identifiers: chr8:g.145639432G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414048G>T , CM000670.2:g.144414048G>T	GRCh38
NC_000008.10:g.145639432G>T , CM000670.1:g.145639432G>T	GRCh37
NC_000008.9:g.145610240G>T	NCBI36
NG_012234.2:g.7843C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1197C>A MANE Select	ENSP00000301305.4:p.Pro399=
ENST00000276833.9:c.1122C>A	ENSP00000276833.5:p.Pro374=
ENST00000301305.7:c.1197C>A	ENSP00000301305.3:p.Pro399=
ENST00000531789.1:n.34C>A
NM_017767.2:c.1122C>A	NP_060237.2:p.Pro374=
NM_130849.3:c.1197C>A	NP_570901.2:p.Pro399=
XM_006716599.1:c.1197C>A	XP_006716662.1:p.Pro399=
XM_011517153.1:c.915C>A	XP_011515455.1:p.Pro305=
XM_024447188.1:c.915C>A	XP_024302956.1:p.Pro305=
XM_024447189.1:c.915C>A	XP_024302957.1:p.Pro305=
NM_001374839.1:c.915C>A	NP_001361768.1:p.Pro305=
NM_017767.3:c.1122C>A	NP_060237.3:p.Pro374=
NM_130849.4:c.1197C>A MANE Select	NP_570901.3:p.Pro399=