Canonical Allele Identifier: CA2782585167

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414415del , CM000670.2:g.144414415del	GRCh38
NC_000008.10:g.145639799del , CM000670.1:g.145639799del	GRCh37
NC_000008.9:g.145610607del	NCBI36
NG_012234.2:g.7477del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.997del MANE Select	ENSP00000301305.4:p.Ala333ProfsTer16
ENST00000276833.9:c.922del	ENSP00000276833.5:p.Ala308ProfsTer16
ENST00000301305.7:c.997del	ENSP00000301305.3:p.Ala333ProfsTer16
NM_017767.2:c.922del	NP_060237.2:p.Ala308ProfsTer16
NM_130849.3:c.997del	NP_570901.2:p.Ala333ProfsTer16
XM_006716599.1:c.997del	XP_006716662.1:p.Ala333ProfsTer16
XM_011517153.1:c.715del	XP_011515455.1:p.Ala239ProfsTer16
XM_024447188.1:c.715del	XP_024302956.1:p.Ala239ProfsTer16
XM_024447189.1:c.715del	XP_024302957.1:p.Ala239ProfsTer16
NM_001374839.1:c.715del	NP_001361768.1:p.Ala239ProfsTer16
NM_017767.3:c.922del	NP_060237.3:p.Ala308ProfsTer16
NM_130849.4:c.997del MANE Select	NP_570901.3:p.Ala333ProfsTer16