Canonical Allele Identifier: CA2295937386
Gene: SLC39A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.36114071_36114072delinsCA , CM000680.2:g.36114071_36114072delinsCA GRCh38
NC_000018.9:g.33694034_33694035delinsCA , CM000680.1:g.33694034_33694035delinsCA GRCh37
NC_000018.8:g.31948032_31948033delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000269187.10:c.1843+25_1843+26delinsTG MANE Select ENSP00000269187.4:n.1843+25_1843+26delins...
ENST00000269187.9:c.1843+25_1843+26delinsTG ENSP00000269187.4:n.1843+25_1843+26delins...
ENST00000440549.6:c.1018+25_1018+26delinsTG ENSP00000401139.1:n.1018+25_1018+26delins...
ENST00000586829.1:c.544+25_544+26delinsTG ENSP00000467724.1:n.544+25_544+26delinsTG...
ENST00000590986.5:c.1843+25_1843+26delinsTG ENSP00000465915.1:n.1843+25_1843+26delins...
NM_001099406.1:c.1018+25_1018+26delinsTG NP_001092876.1:n.1018+25_1018+26delinsTG
NM_012319.3:c.1843+25_1843+26delinsTG NP_036451.3:n.1843+25_1843+26delinsTG
XM_011525900.1:c.1843+25_1843+26delinsTG XP_011524202.1:n.1843+25_1843+26delinsTG
XM_011525901.1:c.1843+25_1843+26delinsTG XP_011524203.1:n.1843+25_1843+26delinsTG
XM_011525900.2:c.1843+25_1843+26delinsTG XP_011524202.1:n.1843+25_1843+26delinsTG
XM_011525901.2:c.1843+25_1843+26delinsTG XP_011524203.1:n.1843+25_1843+26delinsTG
NM_012319.4:c.1843+25_1843+26delinsTG MANE Select NP_036451.4:n.1843+25_1843+26delinsTG
NM_001099406.2:c.1018+25_1018+26delinsTG NP_001092876.1:n.1018+25_1018+26delinsTG