Canonical Allele Identifier: CA1826306891

Gene: SLC39A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414020_144414021delinsCG , CM000670.2:g.144414020_144414021delinsCG	GRCh38
NC_000008.10:g.145639404_145639405delinsCG , CM000670.1:g.145639404_145639405delinsCG	GRCh37
NC_000008.9:g.145610212_145610213delinsCG	NCBI36
NG_012234.2:g.7870_7871delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1224_1225delinsCG MANE Select	ENSP00000301305.4:p.Ala408=
ENST00000276833.9:c.1149_1150delinsCG	ENSP00000276833.5:p.Ala383=
ENST00000301305.7:c.1224_1225delinsCG	ENSP00000301305.3:p.Ala408=
ENST00000531789.1:n.61_62delinsCG
NM_017767.2:c.1149_1150delinsCG	NP_060237.2:p.Ala383=
NM_130849.3:c.1224_1225delinsCG	NP_570901.2:p.Ala408=
XM_006716599.1:c.1224_1225delinsCG	XP_006716662.1:p.Ala408=
XM_011517153.1:c.942_943delinsCG	XP_011515455.1:p.Ala314=
XM_024447188.1:c.942_943delinsCG	XP_024302956.1:p.Ala314=
XM_024447189.1:c.942_943delinsCG	XP_024302957.1:p.Ala314=
NM_001374839.1:c.942_943delinsCG	NP_001361768.1:p.Ala314=
NM_017767.3:c.1149_1150delinsCG	NP_060237.3:p.Ala383=
NM_130849.4:c.1224_1225delinsCG MANE Select	NP_570901.3:p.Ala408=