Canonical Allele Identifier: CA2689098959

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414414-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414414_144414415insTG , CM000670.2:g.144414414_144414415insTG	GRCh38
NC_000008.10:g.145639798_145639799insTG , CM000670.1:g.145639798_145639799insTG	GRCh37
NC_000008.9:g.145610606_145610607insTG	NCBI36
NG_012234.2:g.7476_7477insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.996_997insCA MANE Select	ENSP00000301305.4:p.Ala333GlnfsTer17
ENST00000276833.9:c.921_922insCA	ENSP00000276833.5:p.Ala308GlnfsTer17
ENST00000301305.7:c.996_997insCA	ENSP00000301305.3:p.Ala333GlnfsTer17
NM_017767.2:c.921_922insCA	NP_060237.2:p.Ala308GlnfsTer17
NM_130849.3:c.996_997insCA	NP_570901.2:p.Ala333GlnfsTer17
XM_006716599.1:c.996_997insCA	XP_006716662.1:p.Ala333GlnfsTer17
XM_011517153.1:c.714_715insCA	XP_011515455.1:p.Ala239GlnfsTer17
XM_024447188.1:c.714_715insCA	XP_024302956.1:p.Ala239GlnfsTer17
XM_024447189.1:c.714_715insCA	XP_024302957.1:p.Ala239GlnfsTer17
NM_001374839.1:c.714_715insCA	NP_001361768.1:p.Ala239GlnfsTer17
NM_017767.3:c.921_922insCA	NP_060237.3:p.Ala308GlnfsTer17
NM_130849.4:c.996_997insCA MANE Select	NP_570901.3:p.Ala333GlnfsTer17