Canonical Allele Identifier: CA372620086

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414061-A-T
• MyVariant Identifiers: chr8:g.145639445A>T (hg19) ; chr8:g.144414061A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414061A>T , CM000670.2:g.144414061A>T	GRCh38
NC_000008.10:g.145639445A>T , CM000670.1:g.145639445A>T	GRCh37
NC_000008.9:g.145610253A>T	NCBI36
NG_012234.2:g.7830T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1184T>A MANE Select	ENSP00000301305.4:p.Leu395His
ENST00000276833.9:c.1109T>A	ENSP00000276833.5:p.Leu370His
ENST00000301305.7:c.1184T>A	ENSP00000301305.3:p.Leu395His
ENST00000531789.1:n.21T>A
NM_017767.2:c.1109T>A	NP_060237.2:p.Leu370His
NM_130849.3:c.1184T>A	NP_570901.2:p.Leu395His
XM_006716599.1:c.1184T>A	XP_006716662.1:p.Leu395His
XM_011517153.1:c.902T>A	XP_011515455.1:p.Leu301His
XM_024447188.1:c.902T>A	XP_024302956.1:p.Leu301His
XM_024447189.1:c.902T>A	XP_024302957.1:p.Leu301His
NM_001374839.1:c.902T>A	NP_001361768.1:p.Leu301His
NM_017767.3:c.1109T>A	NP_060237.3:p.Leu370His
NM_130849.4:c.1184T>A MANE Select	NP_570901.3:p.Leu395His