Canonical Allele Identifier: CA2675524405
Gene: SLC23A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139379626T>C , CM000667.2:g.139379626T>C GRCh38
NC_000005.9:g.138715315T>C , CM000667.1:g.138715315T>C GRCh37
NC_000005.8:g.138743214T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348729.8:c.925+52A>G MANE Select ENSP00000302701.4:n.925+52A>G
ENST00000348729.7:c.925+52A>G ENSP00000302701.4:n.925+52A>G
ENST00000353963.7:c.937+52A>G ENSP00000302851.5:n.937+52A>G
ENST00000504513.1:c.165-272A>G
ENST00000506512.1:n.536+52A>G
NM_005847.4:c.925+52A>G NP_005838.3:n.925+52A>G
NM_152685.3:c.937+52A>G NP_689898.2:n.937+52A>G
XM_005272148.3:c.1045+52A>G XP_005272205.3:n.1045+52A>G
XM_005272149.3:c.1033+52A>G XP_005272206.3:n.1033+52A>G
XM_006714741.2:c.1045+52A>G XP_006714804.2:n.1045+52A>G
XM_011543765.1:c.1045+52A>G XP_011542067.1:n.1045+52A>G
XM_011543766.1:c.826+52A>G XP_011542068.1:n.826+52A>G
XM_011543767.1:c.730+52A>G XP_011542069.1:n.730+52A>G
XM_011543768.1:c.610+52A>G XP_011542070.1:n.610+52A>G
XM_011543769.1:c.220+52A>G XP_011542071.1:n.220+52A>G
XM_005272149.4:c.1033+52A>G XP_005272206.3:n.1033+52A>G
XM_011543765.2:c.1045+52A>G XP_011542067.1:n.1045+52A>G
NM_005847.5:c.925+52A>G MANE Select NP_005838.3:n.925+52A>G
NM_152685.4:c.937+52A>G NP_689898.2:n.937+52A>G