Canonical Allele Identifier: CA2689099006

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414479-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414479A>G , CM000670.2:g.144414479A>G	GRCh38
NC_000008.10:g.145639863A>G , CM000670.1:g.145639863A>G	GRCh37
NC_000008.9:g.145610671A>G	NCBI36
NG_012234.2:g.7412T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.977-45T>C MANE Select	ENSP00000301305.4:n.977-45T>C
ENST00000276833.9:c.902-45T>C	ENSP00000276833.5:n.902-45T>C
ENST00000301305.7:c.977-45T>C	ENSP00000301305.3:n.977-45T>C
NM_017767.2:c.902-45T>C	NP_060237.2:n.902-45T>C
NM_130849.3:c.977-45T>C	NP_570901.2:n.977-45T>C
XM_006716599.1:c.977-45T>C	XP_006716662.1:n.977-45T>C
XM_011517153.1:c.695-45T>C	XP_011515455.1:n.695-45T>C
XM_024447188.1:c.695-45T>C	XP_024302956.1:n.695-45T>C
XM_024447189.1:c.695-45T>C	XP_024302957.1:n.695-45T>C
NM_001374839.1:c.695-45T>C	NP_001361768.1:n.695-45T>C
NM_017767.3:c.902-45T>C	NP_060237.3:n.902-45T>C
NM_130849.4:c.977-45T>C MANE Select	NP_570901.3:n.977-45T>C