Canonical Allele Identifier: CA372621214

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414333-T-A
• MyVariant Identifiers: chr8:g.145639717T>A (hg19) ; chr8:g.144414333T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414333T>A , CM000670.2:g.144414333T>A	GRCh38
NC_000008.10:g.145639717T>A , CM000670.1:g.145639717T>A	GRCh37
NC_000008.9:g.145610525T>A	NCBI36
NG_012234.2:g.7558A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1078A>T MANE Select	ENSP00000301305.4:p.Ile360Phe
ENST00000276833.9:c.1003A>T	ENSP00000276833.5:p.Ile335Phe
ENST00000301305.7:c.1078A>T	ENSP00000301305.3:p.Ile360Phe
NM_017767.2:c.1003A>T	NP_060237.2:p.Ile335Phe
NM_130849.3:c.1078A>T	NP_570901.2:p.Ile360Phe
XM_006716599.1:c.1078A>T	XP_006716662.1:p.Ile360Phe
XM_011517153.1:c.796A>T	XP_011515455.1:p.Ile266Phe
XM_024447188.1:c.796A>T	XP_024302956.1:p.Ile266Phe
XM_024447189.1:c.796A>T	XP_024302957.1:p.Ile266Phe
NM_001374839.1:c.796A>T	NP_001361768.1:p.Ile266Phe
NM_017767.3:c.1003A>T	NP_060237.3:p.Ile335Phe
NM_130849.4:c.1078A>T MANE Select	NP_570901.3:p.Ile360Phe