Canonical Allele Identifier: CA463556684

Gene: SLC39A4

Linked Data

• MyVariant Identifiers: chr8:g.145641395C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144416011C>T , CM000670.2:g.144416011C>T	GRCh38
NC_000008.10:g.145641395C>T , CM000670.1:g.145641395C>T	GRCh37
NC_000008.9:g.145612203C>T	NCBI36
NG_012234.2:g.5880G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.273G>A MANE Select	ENSP00000301305.4:p.Arg91=
ENST00000276833.9:c.198G>A	ENSP00000276833.5:p.Arg66=
ENST00000301305.7:c.273G>A	ENSP00000301305.3:p.Arg91=
ENST00000526658.1:c.192+587G>A	ENSP00000434512.1:n.192+587G>A
NM_017767.2:c.198G>A	NP_060237.2:p.Arg66=
NM_130849.3:c.273G>A	NP_570901.2:p.Arg91=
XM_006716599.1:c.273G>A	XP_006716662.1:p.Arg91=
XM_011517153.1:c.192+587G>A	XP_011515455.1:n.192+587G>A
XM_024447188.1:c.192+587G>A	XP_024302956.1:n.192+587G>A
XM_024447189.1:c.192+587G>A	XP_024302957.1:n.192+587G>A
NM_001374839.1:c.192+587G>A	NP_001361768.1:n.192+587G>A
NM_017767.3:c.198G>A	NP_060237.3:p.Arg66=
NM_130849.4:c.273G>A MANE Select	NP_570901.3:p.Arg91=