Canonical Allele Identifier: CA4941754

Gene: SLC39A4

Linked Data

• ClinVar Variation Id: 362261
• ClinVar RCV Id: RCV001510559
• dbSNP Id: rs4355816
• ExAC: 8:145641392 G / A
• gnomAD v2: 8-145641392-G-A
• gnomAD v3: 8-144416008-G-A
• gnomAD v4: 8-144416008-G-A
• MyVariant Identifiers: chr8:g.145641392G>A (hg19) ; chr8:g.144416008G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144416008G>A , CM000670.2:g.144416008G>A	GRCh38
NC_000008.10:g.145641392G>A , CM000670.1:g.145641392G>A	GRCh37
NC_000008.9:g.145612200G>A	NCBI36
NG_012234.2:g.5883C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000301305.8:c.276C>T MANE Select	ENSP00000301305.4:p.Tyr92=
ENST00000276833.9:c.201C>T	ENSP00000276833.5:p.Tyr67=
ENST00000301305.7:c.276C>T	ENSP00000301305.3:p.Tyr92=
ENST00000526658.1:c.193-589C>T	ENSP00000434512.1:n.193-589C>T
NM_017767.2:c.201C>T	NP_060237.2:p.Tyr67=
NM_130849.3:c.276C>T	NP_570901.2:p.Tyr92=
XM_006716599.1:c.276C>T	XP_006716662.1:p.Tyr92=
XM_011517153.1:c.193-589C>T	XP_011515455.1:n.193-589C>T
XM_024447188.1:c.193-589C>T	XP_024302956.1:n.193-589C>T
XM_024447189.1:c.193-589C>T	XP_024302957.1:n.193-589C>T
NM_001374839.1:c.193-589C>T	NP_001361768.1:n.193-589C>T
NM_017767.3:c.201C>T	NP_060237.3:p.Tyr67=
NM_130849.4:c.276C>T MANE Select	NP_570901.3:p.Tyr92=