Canonical Allele Identifier: CA2295937381

Gene: SLC39A6

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36114060_36114062delinsGAA , CM000680.2:g.36114060_36114062delinsGAA	GRCh38
NC_000018.9:g.33694023_33694025delinsGAA , CM000680.1:g.33694023_33694025delinsGAA	GRCh37
NC_000018.8:g.31948021_31948023delinsGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000269187.10:c.1843+35_1843+37delinsTTC MANE Select	ENSP00000269187.4:n.1843+35_1843+37delins...
ENST00000269187.9:c.1843+35_1843+37delinsTTC	ENSP00000269187.4:n.1843+35_1843+37delins...
ENST00000440549.6:c.1018+35_1018+37delinsTTC	ENSP00000401139.1:n.1018+35_1018+37delins...
ENST00000586829.1:c.544+35_544+37delinsTTC	ENSP00000467724.1:n.544+35_544+37delinsTT...
ENST00000590986.5:c.1843+35_1843+37delinsTTC	ENSP00000465915.1:n.1843+35_1843+37delins...
NM_001099406.1:c.1018+35_1018+37delinsTTC	NP_001092876.1:n.1018+35_1018+37delinsTTC...
NM_012319.3:c.1843+35_1843+37delinsTTC	NP_036451.3:n.1843+35_1843+37delinsTTC
XM_011525900.1:c.1843+35_1843+37delinsTTC	XP_011524202.1:n.1843+35_1843+37delinsTTC...
XM_011525901.1:c.1843+35_1843+37delinsTTC	XP_011524203.1:n.1843+35_1843+37delinsTTC...
XM_011525900.2:c.1843+35_1843+37delinsTTC	XP_011524202.1:n.1843+35_1843+37delinsTTC...
XM_011525901.2:c.1843+35_1843+37delinsTTC	XP_011524203.1:n.1843+35_1843+37delinsTTC...
NM_012319.4:c.1843+35_1843+37delinsTTC MANE Select	NP_036451.4:n.1843+35_1843+37delinsTTC
NM_001099406.2:c.1018+35_1018+37delinsTTC	NP_001092876.1:n.1018+35_1018+37delinsTTC...