Canonical Allele Identifier: CA2295937559

Gene: SLC39A6

Linked Data

• dbSNP Id: rs2089328349

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36114522dup , CM000680.2:g.36114522dup	GRCh38
NC_000018.9:g.33694485dup , CM000680.1:g.33694485dup	GRCh37
NC_000018.8:g.31948483dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269187.10:c.1466-47dup MANE Select	ENSP00000269187.4:n.1466-47dup
ENST00000269187.9:c.1466-47dup	ENSP00000269187.4:n.1466-47dup
ENST00000440549.6:c.641-47dup	ENSP00000401139.1:n.641-47dup
ENST00000586829.1:c.167-47dup	ENSP00000467724.1:n.167-47dup
ENST00000590986.5:c.1466-47dup	ENSP00000465915.1:n.1466-47dup
NM_001099406.1:c.641-47dup	NP_001092876.1:n.641-47dup
NM_012319.3:c.1466-47dup	NP_036451.3:n.1466-47dup
XM_011525900.1:c.1466-47dup	XP_011524202.1:n.1466-47dup
XM_011525901.1:c.1466-47dup	XP_011524203.1:n.1466-47dup
XM_011525900.2:c.1466-47dup	XP_011524202.1:n.1466-47dup
XM_011525901.2:c.1466-47dup	XP_011524203.1:n.1466-47dup
NM_012319.4:c.1466-47dup MANE Select	NP_036451.4:n.1466-47dup
NM_001099406.2:c.641-47dup	NP_001092876.1:n.641-47dup