Canonical Allele Identifier: CA2295937382

Gene: SLC39A6

Linked Data

• dbSNP Id: rs2089323073

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36114061_36114062del , CM000680.2:g.36114061_36114062del	GRCh38
NC_000018.9:g.33694024_33694025del , CM000680.1:g.33694024_33694025del	GRCh37
NC_000018.8:g.31948022_31948023del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000269187.10:c.1843+35_1843+36del MANE Select	ENSP00000269187.4:n.1843+35_1843+36del
ENST00000269187.9:c.1843+35_1843+36del	ENSP00000269187.4:n.1843+35_1843+36del
ENST00000440549.6:c.1018+35_1018+36del	ENSP00000401139.1:n.1018+35_1018+36del
ENST00000586829.1:c.544+35_544+36del	ENSP00000467724.1:n.544+35_544+36del
ENST00000590986.5:c.1843+35_1843+36del	ENSP00000465915.1:n.1843+35_1843+36del
NM_001099406.1:c.1018+35_1018+36del	NP_001092876.1:n.1018+35_1018+36del
NM_012319.3:c.1843+35_1843+36del	NP_036451.3:n.1843+35_1843+36del
XM_011525900.1:c.1843+35_1843+36del	XP_011524202.1:n.1843+35_1843+36del
XM_011525901.1:c.1843+35_1843+36del	XP_011524203.1:n.1843+35_1843+36del
XM_011525900.2:c.1843+35_1843+36del	XP_011524202.1:n.1843+35_1843+36del
XM_011525901.2:c.1843+35_1843+36del	XP_011524203.1:n.1843+35_1843+36del
NM_012319.4:c.1843+35_1843+36del MANE Select	NP_036451.4:n.1843+35_1843+36del
NM_001099406.2:c.1018+35_1018+36del	NP_001092876.1:n.1018+35_1018+36del