Canonical Allele Identifier: CA1826307151

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414415_144414416delinsCA , CM000670.2:g.144414415_144414416delinsCA	GRCh38
NC_000008.10:g.145639799_145639800delinsCA , CM000670.1:g.145639799_145639800delinsCA	GRCh37
NC_000008.9:g.145610607_145610608delinsCA	NCBI36
NG_012234.2:g.7475_7476delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.995_996delinsTG MANE Select	ENSP00000301305.4:p.Leu332=
ENST00000276833.9:c.920_921delinsTG	ENSP00000276833.5:p.Leu307=
ENST00000301305.7:c.995_996delinsTG	ENSP00000301305.3:p.Leu332=
NM_017767.2:c.920_921delinsTG	NP_060237.2:p.Leu307=
NM_130849.3:c.995_996delinsTG	NP_570901.2:p.Leu332=
XM_006716599.1:c.995_996delinsTG	XP_006716662.1:p.Leu332=
XM_011517153.1:c.713_714delinsTG	XP_011515455.1:p.Leu238=
XM_024447188.1:c.713_714delinsTG	XP_024302956.1:p.Leu238=
XM_024447189.1:c.713_714delinsTG	XP_024302957.1:p.Leu238=
NM_001374839.1:c.713_714delinsTG	NP_001361768.1:p.Leu238=
NM_017767.3:c.920_921delinsTG	NP_060237.3:p.Leu307=
NM_130849.4:c.995_996delinsTG MANE Select	NP_570901.3:p.Leu332=