Canonical Allele Identifier: CA2641520509

Gene: SLC39A6

Linked Data

• gnomAD v4: 18-36114545-C-CCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36114545_36114546insCTG , CM000680.2:g.36114545_36114546insCTG	GRCh38
NC_000018.9:g.33694508_33694509insCTG , CM000680.1:g.33694508_33694509insCTG	GRCh37
NC_000018.8:g.31948506_31948507insCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269187.10:c.1466-72_1466-71insCAG MANE Select	ENSP00000269187.4:n.1466-72_1466-71insCAG
ENST00000269187.9:c.1466-72_1466-71insCAG	ENSP00000269187.4:n.1466-72_1466-71insCAG
ENST00000440549.6:c.641-72_641-71insCAG	ENSP00000401139.1:n.641-72_641-71insCAG
ENST00000586829.1:c.167-72_167-71insCAG	ENSP00000467724.1:n.167-72_167-71insCAG
ENST00000590986.5:c.1466-72_1466-71insCAG	ENSP00000465915.1:n.1466-72_1466-71insCAG
NM_001099406.1:c.641-72_641-71insCAG	NP_001092876.1:n.641-72_641-71insCAG
NM_012319.3:c.1466-72_1466-71insCAG	NP_036451.3:n.1466-72_1466-71insCAG
XM_011525900.1:c.1466-72_1466-71insCAG	XP_011524202.1:n.1466-72_1466-71insCAG
XM_011525901.1:c.1466-72_1466-71insCAG	XP_011524203.1:n.1466-72_1466-71insCAG
XM_011525900.2:c.1466-72_1466-71insCAG	XP_011524202.1:n.1466-72_1466-71insCAG
XM_011525901.2:c.1466-72_1466-71insCAG	XP_011524203.1:n.1466-72_1466-71insCAG
NM_012319.4:c.1466-72_1466-71insCAG MANE Select	NP_036451.4:n.1466-72_1466-71insCAG
NM_001099406.2:c.641-72_641-71insCAG	NP_001092876.1:n.641-72_641-71insCAG