Canonical Allele Identifier: CA372621141

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414297-C-T
• MyVariant Identifiers: chr8:g.144414297C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414297C>T , CM000670.2:g.144414297C>T	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1114G>A MANE Select	ENSP00000301305.4:p.Val372Ile
ENST00000276833.9:c.1039G>A	ENSP00000276833.5:p.Val347Ile
ENST00000301305.7:c.1114G>A	ENSP00000301305.3:p.Val372Ile
XM_006716599.1:c.1114G>A	XP_006716662.1:p.Val372Ile
XM_011517153.1:c.832G>A	XP_011515455.1:p.Val278Ile
XM_024447188.1:c.832G>A	XP_024302956.1:p.Val278Ile
XM_024447189.1:c.832G>A	XP_024302957.1:p.Val278Ile
NM_001374839.1:c.832G>A	NP_001361768.1:p.Val278Ile
NM_017767.3:c.1039G>A	NP_060237.3:p.Val347Ile
NM_130849.4:c.1114G>A MANE Select	NP_570901.3:p.Val372Ile