Canonical Allele Identifier: CA459904503

Gene: SLC39A14

Linked Data

• gnomAD v4: 8-22408336-T-C
• MyVariant Identifiers: chr8:g.22265849T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22408336T>C , CM000670.2:g.22408336T>C	GRCh38
NC_000008.10:g.22265849T>C , CM000670.1:g.22265849T>C	GRCh37
NC_000008.9:g.22321794T>C	NCBI36
NG_054890.1:g.46088T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359741.10:c.297T>C MANE Plus Clinical	ENSP00000352779.5:p.Thr99=
ENST00000381237.6:c.297T>C MANE Select	ENSP00000370635.1:p.Thr99=
ENST00000240095.10:c.297T>C	ENSP00000240095.6:p.Thr99=
ENST00000289952.9:c.297T>C	ENSP00000289952.5:p.Thr99=
ENST00000359741.9:c.297T>C	ENSP00000352779.5:p.Thr99=
ENST00000381237.5:c.297T>C	ENSP00000370635.1:p.Thr99=
ENST00000517552.1:c.297T>C	ENSP00000430564.1:p.Thr99=
ENST00000519960.5:c.297T>C	ENSP00000430629.1:p.Thr99=
ENST00000522881.2:c.297T>C	ENSP00000429328.2:p.Thr99=
NM_001128431.2:c.297T>C	NP_001121903.1:p.Thr99=
NM_001135153.1:c.297T>C	NP_001128625.1:p.Thr99=
NM_001135154.1:c.297T>C	NP_001128626.1:p.Thr99=
NM_015359.4:c.297T>C	NP_056174.2:p.Thr99=
XM_005273463.1:c.327T>C	XP_005273520.1:p.Thr109=
XM_005273465.1:c.297T>C	XP_005273522.1:p.Thr99=
XM_005273466.3:c.297T>C	XP_005273523.1:p.Thr99=
XM_006716323.1:c.327T>C	XP_006716386.1:p.Thr109=
XM_006716324.1:c.297T>C	XP_006716387.1:p.Thr99=
XM_011544477.1:c.297T>C	XP_011542779.1:p.Thr99=
XM_011544478.1:c.297T>C	XP_011542780.1:p.Thr99=
NM_001128431.3:c.297T>C	NP_001121903.1:p.Thr99=
NM_001135153.2:c.297T>C	NP_001128625.1:p.Thr99=
NM_001135154.2:c.297T>C	NP_001128626.1:p.Thr99=
NM_001351655.1:c.297T>C	NP_001338584.1:p.Thr99=
NM_001351656.1:c.297T>C	NP_001338585.1:p.Thr99=
NM_001351657.1:c.327T>C	NP_001338586.1:p.Thr109=
NM_001351658.1:c.327T>C	NP_001338587.1:p.Thr109=
NM_001351659.1:c.327T>C	NP_001338588.1:p.Thr109=
NM_001351660.1:c.297T>C	NP_001338589.1:p.Thr99=
NM_015359.5:c.297T>C	NP_056174.2:p.Thr99=
XM_005273466.4:c.297T>C	XP_005273523.1:p.Thr99=
XM_006716324.3:c.297T>C	XP_006716387.1:p.Thr99=
XM_011544478.3:c.297T>C	XP_011542780.1:p.Thr99=
XM_017013293.2:c.327T>C	XP_016868782.1:p.Thr109=
NM_001128431.4:c.297T>C MANE Select	NP_001121903.1:p.Thr99=
NM_001135153.3:c.297T>C	NP_001128625.1:p.Thr99=
NM_001135154.3:c.297T>C	NP_001128626.1:p.Thr99=
NM_001351655.2:c.297T>C	NP_001338584.1:p.Thr99=
NM_001351656.2:c.297T>C	NP_001338585.1:p.Thr99=
NM_001351657.2:c.327T>C	NP_001338586.1:p.Thr109=
NM_001351658.2:c.327T>C	NP_001338587.1:p.Thr109=
NM_001351659.2:c.327T>C	NP_001338588.1:p.Thr109=
NM_001351660.2:c.297T>C	NP_001338589.1:p.Thr99=
NM_015359.6:c.297T>C MANE Plus Clinical	NP_056174.2:p.Thr99=