Canonical Allele Identifier: CA372621419

Gene: SLC39A4

Linked Data

• dbSNP Id: rs1822078302
• gnomAD v3: 8-144414436-T-A
• gnomAD v4: 8-144414436-T-A
• MyVariant Identifiers: chr8:g.145639820T>A (hg19) ; chr8:g.144414436T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414436T>A , CM000670.2:g.144414436T>A	GRCh38
NC_000008.10:g.145639820T>A , CM000670.1:g.145639820T>A	GRCh37
NC_000008.9:g.145610628T>A	NCBI36
NG_012234.2:g.7455A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.977-2A>T MANE Select	ENSP00000301305.4:n.977-2A>T
ENST00000276833.9:c.902-2A>T	ENSP00000276833.5:n.902-2A>T
ENST00000301305.7:c.977-2A>T	ENSP00000301305.3:n.977-2A>T
NM_017767.2:c.902-2A>T	NP_060237.2:n.902-2A>T
NM_130849.3:c.977-2A>T	NP_570901.2:n.977-2A>T
XM_006716599.1:c.977-2A>T	XP_006716662.1:n.977-2A>T
XM_011517153.1:c.695-2A>T	XP_011515455.1:n.695-2A>T
XM_024447188.1:c.695-2A>T	XP_024302956.1:n.695-2A>T
XM_024447189.1:c.695-2A>T	XP_024302957.1:n.695-2A>T
NM_001374839.1:c.695-2A>T	NP_001361768.1:n.695-2A>T
NM_017767.3:c.902-2A>T	NP_060237.3:n.902-2A>T
NM_130849.4:c.977-2A>T MANE Select	NP_570901.3:n.977-2A>T