Canonical Allele Identifier: CA503641314

Gene: SLC39A6

Linked Data

• MyVariant Identifiers: chr18:g.33694388A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.36114425A>G , CM000680.2:g.36114425A>G	GRCh38
NC_000018.9:g.33694388A>G , CM000680.1:g.33694388A>G	GRCh37
NC_000018.8:g.31948386A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269187.10:c.1515T>C MANE Select	ENSP00000269187.4:p.Asp505=
ENST00000269187.9:c.1515T>C	ENSP00000269187.4:p.Asp505=
ENST00000440549.6:c.690T>C	ENSP00000401139.1:p.Asp230=
ENST00000586829.1:c.216T>C	ENSP00000467724.1:p.Asp72=
ENST00000590986.5:c.1515T>C	ENSP00000465915.1:p.Asp505=
NM_001099406.1:c.690T>C	NP_001092876.1:p.Asp230=
NM_012319.3:c.1515T>C	NP_036451.3:p.Asp505=
XM_011525900.1:c.1515T>C	XP_011524202.1:p.Asp505=
XM_011525901.1:c.1515T>C	XP_011524203.1:p.Asp505=
XM_011525900.2:c.1515T>C	XP_011524202.1:p.Asp505=
XM_011525901.2:c.1515T>C	XP_011524203.1:p.Asp505=
NM_012319.4:c.1515T>C MANE Select	NP_036451.4:p.Asp505=
NM_001099406.2:c.690T>C	NP_001092876.1:p.Asp230=