Canonical Allele Identifier: CA372621368

Gene: SLC39A4

Linked Data

• MyVariant Identifiers: chr8:g.145639795T>C (hg19) ; chr8:g.144414411T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414411T>C , CM000670.2:g.144414411T>C	GRCh38
NC_000008.10:g.145639795T>C , CM000670.1:g.145639795T>C	GRCh37
NC_000008.9:g.145610603T>C	NCBI36
NG_012234.2:g.7480A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1000A>G MANE Select	ENSP00000301305.4:p.Thr334Ala
ENST00000276833.9:c.925A>G	ENSP00000276833.5:p.Thr309Ala
ENST00000301305.7:c.1000A>G	ENSP00000301305.3:p.Thr334Ala
NM_017767.2:c.925A>G	NP_060237.2:p.Thr309Ala
NM_130849.3:c.1000A>G	NP_570901.2:p.Thr334Ala
XM_006716599.1:c.1000A>G	XP_006716662.1:p.Thr334Ala
XM_011517153.1:c.718A>G	XP_011515455.1:p.Thr240Ala
XM_024447188.1:c.718A>G	XP_024302956.1:p.Thr240Ala
XM_024447189.1:c.718A>G	XP_024302957.1:p.Thr240Ala
NM_001374839.1:c.718A>G	NP_001361768.1:p.Thr240Ala
NM_017767.3:c.925A>G	NP_060237.3:p.Thr309Ala
NM_130849.4:c.1000A>G MANE Select	NP_570901.3:p.Thr334Ala