Canonical Allele Identifier: CA2174120372

Gene: SLC30A4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45508837T= , CM000677.2:g.45508837T=	GRCh38
NC_000015.9:g.45801035T= , CM000677.1:g.45801035T=	GRCh37
NC_000015.8:g.43588327T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261867.5:c.538+2301A= MANE Select	ENSP00000261867.3:n.538+2301A=
ENST00000261867.4:c.538+2301A=	ENSP00000261867.3:n.538+2301A=
ENST00000559667.2:n.420+2301A=
NM_013309.4:c.538+2301A=	NP_037441.2:n.538+2301A=
XM_011521997.1:c.538+2301A=	XP_011520299.1:n.538+2301A=
NM_001321036.1:c.538+2301A=	NP_001307965.1:n.538+2301A=
NM_013309.5:c.538+2301A=	NP_037441.2:n.538+2301A=
XM_011521997.3:c.538+2301A=	XP_011520299.1:n.538+2301A=
XM_017022560.2:c.538+2301A=	XP_016878049.1:n.538+2301A=
NM_013309.6:c.538+2301A= MANE Select	NP_037441.2:n.538+2301A=
NM_001321036.2:c.538+2301A=	NP_001307965.1:n.538+2301A=