Canonical Allele Identifier: CA2812111274

Gene: SLC39A6

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36114541A>T , CM000680.2:g.36114541A>T	GRCh38
NC_000018.9:g.33694504A>T , CM000680.1:g.33694504A>T	GRCh37
NC_000018.8:g.31948502A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269187.10:c.1466-67T>A MANE Select	ENSP00000269187.4:n.1466-67T>A
ENST00000269187.9:c.1466-67T>A	ENSP00000269187.4:n.1466-67T>A
ENST00000440549.6:c.641-67T>A	ENSP00000401139.1:n.641-67T>A
ENST00000586829.1:c.167-67T>A	ENSP00000467724.1:n.167-67T>A
ENST00000590986.5:c.1466-67T>A	ENSP00000465915.1:n.1466-67T>A
NM_001099406.1:c.641-67T>A	NP_001092876.1:n.641-67T>A
NM_012319.3:c.1466-67T>A	NP_036451.3:n.1466-67T>A
XM_011525900.1:c.1466-67T>A	XP_011524202.1:n.1466-67T>A
XM_011525901.1:c.1466-67T>A	XP_011524203.1:n.1466-67T>A
XM_011525900.2:c.1466-67T>A	XP_011524202.1:n.1466-67T>A
XM_011525901.2:c.1466-67T>A	XP_011524203.1:n.1466-67T>A
NM_012319.4:c.1466-67T>A MANE Select	NP_036451.4:n.1466-67T>A
NM_001099406.2:c.641-67T>A	NP_001092876.1:n.641-67T>A