Canonical Allele Identifier: CA2689097816

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414103-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414104dup , CM000670.2:g.144414104dup	GRCh38
NC_000008.10:g.145639488dup , CM000670.1:g.145639488dup	GRCh37
NC_000008.9:g.145610296dup	NCBI36
NG_012234.2:g.7787dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1150-9dup MANE Select	ENSP00000301305.4:n.1150-9dup
ENST00000276833.9:c.1075-9dup	ENSP00000276833.5:n.1075-9dup
ENST00000301305.7:c.1150-9dup	ENSP00000301305.3:n.1150-9dup
NM_017767.2:c.1075-9dup	NP_060237.2:n.1075-9dup
NM_130849.3:c.1150-9dup	NP_570901.2:n.1150-9dup
XM_006716599.1:c.1150-9dup	XP_006716662.1:n.1150-9dup
XM_011517153.1:c.868-9dup	XP_011515455.1:n.868-9dup
XM_024447188.1:c.868-9dup	XP_024302956.1:n.868-9dup
XM_024447189.1:c.868-9dup	XP_024302957.1:n.868-9dup
NM_001374839.1:c.868-9dup	NP_001361768.1:n.868-9dup
NM_017767.3:c.1075-9dup	NP_060237.3:n.1075-9dup
NM_130849.4:c.1150-9dup MANE Select	NP_570901.3:n.1150-9dup