Canonical Allele Identifier: CA298701291

Gene: SLC39A6

Linked Data

• dbSNP Id: rs35107919
• MyVariant Identifiers: chr18:g.33694494_33694495insC (hg19) ; chr18:g.36114531_36114532insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36114531_36114532insC , CM000680.2:g.36114531_36114532insC	GRCh38
NC_000018.9:g.33694494_33694495insC , CM000680.1:g.33694494_33694495insC	GRCh37
NC_000018.8:g.31948492_31948493insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269187.10:c.1466-58_1466-57insG MANE Select	ENSP00000269187.4:n.1466-58_1466-57insG
ENST00000269187.9:c.1466-58_1466-57insG	ENSP00000269187.4:n.1466-58_1466-57insG
ENST00000440549.6:c.641-58_641-57insG	ENSP00000401139.1:n.641-58_641-57insG
ENST00000586829.1:c.167-58_167-57insG	ENSP00000467724.1:n.167-58_167-57insG
ENST00000590986.5:c.1466-58_1466-57insG	ENSP00000465915.1:n.1466-58_1466-57insG
NM_001099406.1:c.641-58_641-57insG	NP_001092876.1:n.641-58_641-57insG
NM_012319.3:c.1466-58_1466-57insG	NP_036451.3:n.1466-58_1466-57insG
XM_011525900.1:c.1466-58_1466-57insG	XP_011524202.1:n.1466-58_1466-57insG
XM_011525901.1:c.1466-58_1466-57insG	XP_011524203.1:n.1466-58_1466-57insG
XM_011525900.2:c.1466-58_1466-57insG	XP_011524202.1:n.1466-58_1466-57insG
XM_011525901.2:c.1466-58_1466-57insG	XP_011524203.1:n.1466-58_1466-57insG
NM_012319.4:c.1466-58_1466-57insG MANE Select	NP_036451.4:n.1466-58_1466-57insG
NM_001099406.2:c.641-58_641-57insG	NP_001092876.1:n.641-58_641-57insG