Canonical Allele Identifier: CA2295937502

Gene: SLC39A6

Linked Data

• dbSNP Id: rs2089326702

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36114391_36114392insTA , CM000680.2:g.36114391_36114392insTA	GRCh38
NC_000018.9:g.33694354_33694355insTA , CM000680.1:g.33694354_33694355insTA	GRCh37
NC_000018.8:g.31948352_31948353insTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269187.10:c.1548_1549insTA MANE Select	ENSP00000269187.4:p.Val517Ter
ENST00000269187.9:c.1548_1549insTA	ENSP00000269187.4:p.Val517Ter
ENST00000440549.6:c.723_724insTA	ENSP00000401139.1:p.Val242Ter
ENST00000586829.1:c.249_250insTA	ENSP00000467724.1:p.Val84Ter
ENST00000590986.5:c.1548_1549insTA	ENSP00000465915.1:p.Val517Ter
NM_001099406.1:c.723_724insTA	NP_001092876.1:p.Val242Ter
NM_012319.3:c.1548_1549insTA	NP_036451.3:p.Val517Ter
XM_011525900.1:c.1548_1549insTA	XP_011524202.1:p.Val517Ter
XM_011525901.1:c.1548_1549insTA	XP_011524203.1:p.Val517Ter
XM_011525900.2:c.1548_1549insTA	XP_011524202.1:p.Val517Ter
XM_011525901.2:c.1548_1549insTA	XP_011524203.1:p.Val517Ter
NM_012319.4:c.1548_1549insTA MANE Select	NP_036451.4:p.Val517Ter
NM_001099406.2:c.723_724insTA	NP_001092876.1:p.Val242Ter