Canonical Allele Identifier: CA372619826

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414014-A-G
• MyVariant Identifiers: chr8:g.145639398A>G (hg19) ; chr8:g.144414014A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414014A>G , CM000670.2:g.144414014A>G	GRCh38
NC_000008.10:g.145639398A>G , CM000670.1:g.145639398A>G	GRCh37
NC_000008.9:g.145610206A>G	NCBI36
NG_012234.2:g.7877T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1231T>C MANE Select	ENSP00000301305.4:p.Tyr411His
ENST00000276833.9:c.1156T>C	ENSP00000276833.5:p.Tyr386His
ENST00000301305.7:c.1231T>C	ENSP00000301305.3:p.Tyr411His
ENST00000531789.1:n.68T>C
NM_017767.2:c.1156T>C	NP_060237.2:p.Tyr386His
NM_130849.3:c.1231T>C	NP_570901.2:p.Tyr411His
XM_006716599.1:c.1231T>C	XP_006716662.1:p.Tyr411His
XM_011517153.1:c.949T>C	XP_011515455.1:p.Tyr317His
XM_024447188.1:c.949T>C	XP_024302956.1:p.Tyr317His
XM_024447189.1:c.949T>C	XP_024302957.1:p.Tyr317His
NM_001374839.1:c.949T>C	NP_001361768.1:p.Tyr317His
NM_017767.3:c.1156T>C	NP_060237.3:p.Tyr386His
NM_130849.4:c.1231T>C MANE Select	NP_570901.3:p.Tyr411His