Canonical Allele Identifier: CA372621236

Gene: SLC39A4

Linked Data

• MyVariant Identifiers: chr8:g.145639728A>G (hg19) ; chr8:g.144414344A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414344A>G , CM000670.2:g.144414344A>G	GRCh38
NC_000008.10:g.145639728A>G , CM000670.1:g.145639728A>G	GRCh37
NC_000008.9:g.145610536A>G	NCBI36
NG_012234.2:g.7547T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1067T>C MANE Select	ENSP00000301305.4:p.Val356Ala
ENST00000276833.9:c.992T>C	ENSP00000276833.5:p.Val331Ala
ENST00000301305.7:c.1067T>C	ENSP00000301305.3:p.Val356Ala
NM_017767.2:c.992T>C	NP_060237.2:p.Val331Ala
NM_130849.3:c.1067T>C	NP_570901.2:p.Val356Ala
XM_006716599.1:c.1067T>C	XP_006716662.1:p.Val356Ala
XM_011517153.1:c.785T>C	XP_011515455.1:p.Val262Ala
XM_024447188.1:c.785T>C	XP_024302956.1:p.Val262Ala
XM_024447189.1:c.785T>C	XP_024302957.1:p.Val262Ala
NM_001374839.1:c.785T>C	NP_001361768.1:p.Val262Ala
NM_017767.3:c.992T>C	NP_060237.3:p.Val331Ala
NM_130849.4:c.1067T>C MANE Select	NP_570901.3:p.Val356Ala