Canonical Allele Identifier: CA2675524417

Gene: SLC23A1

Linked Data

• gnomAD v4: 5-139379642-AGTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379644_139379646del , CM000667.2:g.139379644_139379646del	GRCh38
NC_000005.9:g.138715333_138715335del , CM000667.1:g.138715333_138715335del	GRCh37
NC_000005.8:g.138743232_138743234del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.925+33_925+35del MANE Select	ENSP00000302701.4:n.925+33_925+35del
ENST00000348729.7:c.925+33_925+35del	ENSP00000302701.4:n.925+33_925+35del
ENST00000353963.7:c.937+33_937+35del	ENSP00000302851.5:n.937+33_937+35del
ENST00000504513.1:c.165-291_165-289del
ENST00000506512.1:n.536+33_536+35del
NM_005847.4:c.925+33_925+35del	NP_005838.3:n.925+33_925+35del
NM_152685.3:c.937+33_937+35del	NP_689898.2:n.937+33_937+35del
XM_005272148.3:c.1045+33_1045+35del	XP_005272205.3:n.1045+33_1045+35del
XM_005272149.3:c.1033+33_1033+35del	XP_005272206.3:n.1033+33_1033+35del
XM_006714741.2:c.1045+33_1045+35del	XP_006714804.2:n.1045+33_1045+35del
XM_011543765.1:c.1045+33_1045+35del	XP_011542067.1:n.1045+33_1045+35del
XM_011543766.1:c.826+33_826+35del	XP_011542068.1:n.826+33_826+35del
XM_011543767.1:c.730+33_730+35del	XP_011542069.1:n.730+33_730+35del
XM_011543768.1:c.610+33_610+35del	XP_011542070.1:n.610+33_610+35del
XM_011543769.1:c.220+33_220+35del	XP_011542071.1:n.220+33_220+35del
XM_005272149.4:c.1033+33_1033+35del	XP_005272206.3:n.1033+33_1033+35del
XM_011543765.2:c.1045+33_1045+35del	XP_011542067.1:n.1045+33_1045+35del
NM_005847.5:c.925+33_925+35del MANE Select	NP_005838.3:n.925+33_925+35del
NM_152685.4:c.937+33_937+35del	NP_689898.2:n.937+33_937+35del