Canonical Allele Identifier: CA372620249

Gene: SLC39A4

Linked Data

• MyVariant Identifiers: chr8:g.145639473C>G (hg19) ; chr8:g.144414089C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414089C>G , CM000670.2:g.144414089C>G	GRCh38
NC_000008.10:g.145639473C>G , CM000670.1:g.145639473C>G	GRCh37
NC_000008.9:g.145610281C>G	NCBI36
NG_012234.2:g.7802G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1156G>C MANE Select	ENSP00000301305.4:p.Gly386Arg
ENST00000276833.9:c.1081G>C	ENSP00000276833.5:p.Gly361Arg
ENST00000301305.7:c.1156G>C	ENSP00000301305.3:p.Gly386Arg
NM_017767.2:c.1081G>C	NP_060237.2:p.Gly361Arg
NM_130849.3:c.1156G>C	NP_570901.2:p.Gly386Arg
XM_006716599.1:c.1156G>C	XP_006716662.1:p.Gly386Arg
XM_011517153.1:c.874G>C	XP_011515455.1:p.Gly292Arg
XM_024447188.1:c.874G>C	XP_024302956.1:p.Gly292Arg
XM_024447189.1:c.874G>C	XP_024302957.1:p.Gly292Arg
NM_001374839.1:c.874G>C	NP_001361768.1:p.Gly292Arg
NM_017767.3:c.1081G>C	NP_060237.3:p.Gly361Arg
NM_130849.4:c.1156G>C MANE Select	NP_570901.3:p.Gly386Arg