Canonical Allele Identifier: CA372621375

Gene: SLC39A4

Linked Data

• dbSNP Id: rs1822076429
• gnomAD v3: 8-144414414-C-T
• gnomAD v4: 8-144414414-C-T
• MyVariant Identifiers: chr8:g.145639798C>T (hg19) ; chr8:g.144414414C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414414C>T , CM000670.2:g.144414414C>T	GRCh38
NC_000008.10:g.145639798C>T , CM000670.1:g.145639798C>T	GRCh37
NC_000008.9:g.145610606C>T	NCBI36
NG_012234.2:g.7477G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.997G>A MANE Select	ENSP00000301305.4:p.Ala333Thr
ENST00000276833.9:c.922G>A	ENSP00000276833.5:p.Ala308Thr
ENST00000301305.7:c.997G>A	ENSP00000301305.3:p.Ala333Thr
NM_017767.2:c.922G>A	NP_060237.2:p.Ala308Thr
NM_130849.3:c.997G>A	NP_570901.2:p.Ala333Thr
XM_006716599.1:c.997G>A	XP_006716662.1:p.Ala333Thr
XM_011517153.1:c.715G>A	XP_011515455.1:p.Ala239Thr
XM_024447188.1:c.715G>A	XP_024302956.1:p.Ala239Thr
XM_024447189.1:c.715G>A	XP_024302957.1:p.Ala239Thr
NM_001374839.1:c.715G>A	NP_001361768.1:p.Ala239Thr
NM_017767.3:c.922G>A	NP_060237.3:p.Ala308Thr
NM_130849.4:c.997G>A MANE Select	NP_570901.3:p.Ala333Thr