Canonical Allele Identifier: CA372621142

Gene: SLC39A4

Linked Data

• gnomAD v4: 8-144414299-G-A
• MyVariant Identifiers: chr8:g.145639683G>A (hg19) ; chr8:g.144414299G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414299G>A , CM000670.2:g.144414299G>A	GRCh38
NC_000008.10:g.145639683G>A , CM000670.1:g.145639683G>A	GRCh37
NC_000008.9:g.145610491G>A	NCBI36
NG_012234.2:g.7592C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1112C>T MANE Select	ENSP00000301305.4:p.Ala371Val
ENST00000276833.9:c.1037C>T	ENSP00000276833.5:p.Ala346Val
ENST00000301305.7:c.1112C>T	ENSP00000301305.3:p.Ala371Val
NM_017767.2:c.1037C>T	NP_060237.2:p.Ala346Val
NM_130849.3:c.1112C>T	NP_570901.2:p.Ala371Val
XM_006716599.1:c.1112C>T	XP_006716662.1:p.Ala371Val
XM_011517153.1:c.830C>T	XP_011515455.1:p.Ala277Val
XM_024447188.1:c.830C>T	XP_024302956.1:p.Ala277Val
XM_024447189.1:c.830C>T	XP_024302957.1:p.Ala277Val
NM_001374839.1:c.830C>T	NP_001361768.1:p.Ala277Val
NM_017767.3:c.1037C>T	NP_060237.3:p.Ala346Val
NM_130849.4:c.1112C>T MANE Select	NP_570901.3:p.Ala371Val