Canonical Allele Identifier: CA2675524398

Gene: SLC23A1

Linked Data

• gnomAD v4: 5-139379616-C-CAGGAGTCTGTCTCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379620_139379634dup , CM000667.2:g.139379620_139379634dup	GRCh38
NC_000005.9:g.138715309_138715323dup , CM000667.1:g.138715309_138715323dup	GRCh37
NC_000005.8:g.138743208_138743222dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.925+47_925+61dup MANE Select	ENSP00000302701.4:n.925+47_925+61dup
ENST00000348729.7:c.925+47_925+61dup	ENSP00000302701.4:n.925+47_925+61dup
ENST00000353963.7:c.937+47_937+61dup	ENSP00000302851.5:n.937+47_937+61dup
ENST00000504513.1:c.165-277_165-263dup
ENST00000506512.1:n.536+47_536+61dup
NM_005847.4:c.925+47_925+61dup	NP_005838.3:n.925+47_925+61dup
NM_152685.3:c.937+47_937+61dup	NP_689898.2:n.937+47_937+61dup
XM_005272148.3:c.1045+47_1045+61dup	XP_005272205.3:n.1045+47_1045+61dup
XM_005272149.3:c.1033+47_1033+61dup	XP_005272206.3:n.1033+47_1033+61dup
XM_006714741.2:c.1045+47_1045+61dup	XP_006714804.2:n.1045+47_1045+61dup
XM_011543765.1:c.1045+47_1045+61dup	XP_011542067.1:n.1045+47_1045+61dup
XM_011543766.1:c.826+47_826+61dup	XP_011542068.1:n.826+47_826+61dup
XM_011543767.1:c.730+47_730+61dup	XP_011542069.1:n.730+47_730+61dup
XM_011543768.1:c.610+47_610+61dup	XP_011542070.1:n.610+47_610+61dup
XM_011543769.1:c.220+47_220+61dup	XP_011542071.1:n.220+47_220+61dup
XM_005272149.4:c.1033+47_1033+61dup	XP_005272206.3:n.1033+47_1033+61dup
XM_011543765.2:c.1045+47_1045+61dup	XP_011542067.1:n.1045+47_1045+61dup
NM_005847.5:c.925+47_925+61dup MANE Select	NP_005838.3:n.925+47_925+61dup
NM_152685.4:c.937+47_937+61dup	NP_689898.2:n.937+47_937+61dup