Canonical Allele Identifier: CA463449678

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414361-G-A
• MyVariant Identifiers: chr8:g.145639745G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414361G>A , CM000670.2:g.144414361G>A	GRCh38
NC_000008.10:g.145639745G>A , CM000670.1:g.145639745G>A	GRCh37
NC_000008.9:g.145610553G>A	NCBI36
NG_012234.2:g.7530C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1050C>T MANE Select	ENSP00000301305.4:p.Cys350=
ENST00000276833.9:c.975C>T	ENSP00000276833.5:p.Cys325=
ENST00000301305.7:c.1050C>T	ENSP00000301305.3:p.Cys350=
NM_017767.2:c.975C>T	NP_060237.2:p.Cys325=
NM_130849.3:c.1050C>T	NP_570901.2:p.Cys350=
XM_006716599.1:c.1050C>T	XP_006716662.1:p.Cys350=
XM_011517153.1:c.768C>T	XP_011515455.1:p.Cys256=
XM_024447188.1:c.768C>T	XP_024302956.1:p.Cys256=
XM_024447189.1:c.768C>T	XP_024302957.1:p.Cys256=
NM_001374839.1:c.768C>T	NP_001361768.1:p.Cys256=
NM_017767.3:c.975C>T	NP_060237.3:p.Cys325=
NM_130849.4:c.1050C>T MANE Select	NP_570901.3:p.Cys350=