Canonical Allele Identifier: CA778833577

Gene: SLC39A6

Linked Data

• dbSNP Id: rs1458919271
• gnomAD v4: 18-36113953-TAAAAGA-T
• MyVariant Identifiers: chr18:g.33693917_33693922del (hg19) ; chr18:g.36113954_36113959del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36113959_36113964del , CM000680.2:g.36113959_36113964del	GRCh38
NC_000018.9:g.33693922_33693927del , CM000680.1:g.33693922_33693927del	GRCh37
NC_000018.8:g.31947920_31947925del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269187.10:c.1843+138_1843+143del MANE Select	ENSP00000269187.4:n.1843+138_1843+143del
ENST00000269187.9:c.1843+138_1843+143del	ENSP00000269187.4:n.1843+138_1843+143del
ENST00000440549.6:c.1018+138_1018+143del	ENSP00000401139.1:n.1018+138_1018+143del
ENST00000586829.1:c.544+138_544+143del	ENSP00000467724.1:n.544+138_544+143del
ENST00000590986.5:c.1843+138_1843+143del	ENSP00000465915.1:n.1843+138_1843+143del
NM_001099406.1:c.1018+138_1018+143del	NP_001092876.1:n.1018+138_1018+143del
NM_012319.3:c.1843+138_1843+143del	NP_036451.3:n.1843+138_1843+143del
XM_011525900.1:c.1843+138_1843+143del	XP_011524202.1:n.1843+138_1843+143del
XM_011525901.1:c.1843+138_1843+143del	XP_011524203.1:n.1843+138_1843+143del
XM_011525900.2:c.1843+138_1843+143del	XP_011524202.1:n.1843+138_1843+143del
XM_011525901.2:c.1843+138_1843+143del	XP_011524203.1:n.1843+138_1843+143del
NM_012319.4:c.1843+138_1843+143del MANE Select	NP_036451.4:n.1843+138_1843+143del
NM_001099406.2:c.1018+138_1018+143del	NP_001092876.1:n.1018+138_1018+143del