Canonical Allele Identifier: CA463556677

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144416005-G-C
• MyVariant Identifiers: chr8:g.145641389G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144416005G>C , CM000670.2:g.144416005G>C	GRCh38
NC_000008.10:g.145641389G>C , CM000670.1:g.145641389G>C	GRCh37
NC_000008.9:g.145612197G>C	NCBI36
NG_012234.2:g.5886C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000301305.8:c.279C>G MANE Select	ENSP00000301305.4:p.Val93=
ENST00000276833.9:c.204C>G	ENSP00000276833.5:p.Val68=
ENST00000301305.7:c.279C>G	ENSP00000301305.3:p.Val93=
ENST00000526658.1:c.193-586C>G	ENSP00000434512.1:n.193-586C>G
NM_017767.2:c.204C>G	NP_060237.2:p.Val68=
NM_130849.3:c.279C>G	NP_570901.2:p.Val93=
XM_006716599.1:c.279C>G	XP_006716662.1:p.Val93=
XM_011517153.1:c.193-586C>G	XP_011515455.1:n.193-586C>G
XM_024447188.1:c.193-586C>G	XP_024302956.1:n.193-586C>G
XM_024447189.1:c.193-586C>G	XP_024302957.1:n.193-586C>G
NM_001374839.1:c.193-586C>G	NP_001361768.1:n.193-586C>G
NM_017767.3:c.204C>G	NP_060237.3:p.Val68=
NM_130849.4:c.279C>G MANE Select	NP_570901.3:p.Val93=