Canonical Allele Identifier: CA2662328537
Gene: SLC40A1 HGNC NCBI

Linked Data

gnomAD v4: 2-189563485-C-CTTA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563485_189563486insTTA , CM000664.2:g.189563485_189563486insTTA GRCh38
NC_000002.11:g.190428211_190428212insTTA , CM000664.1:g.190428211_190428212insTTA GRCh37
NC_000002.10:g.190136456_190136457insTTA NCBI36
NG_009027.1:g.22326_22327insTAA , LRG_837:g.22326_22327insTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1402+98_1402+99insTAA MANE Select ENSP00000261024.3:n.1402+98_1402+99insTAA
ENST00000261024.6:c.1402+98_1402+99insTAA ENSP00000261024.2:n.1402+98_1402+99insTAA
NM_014585.5:c.1402+98_1402+99insTAA , LRG_837t1:c.1402+98_1402+99insTAA NP_055400.1:n.1402+98_1402+99insTAA
XM_005246505.1:c.1282+98_1282+99insTAA XP_005246562.1:n.1282+98_1282+99insTAA
XM_005246505.2:c.1282+98_1282+99insTAA XP_005246562.1:n.1282+98_1282+99insTAA
XM_017003938.2:c.1282+98_1282+99insTAA XP_016859427.1:n.1282+98_1282+99insTAA
NM_014585.6:c.1402+98_1402+99insTAA MANE Select NP_055400.1:n.1402+98_1402+99insTAA
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