Canonical Allele Identifier: CA1315654553
Gene: SLC40A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564243C= , CM000664.2:g.189564243C= GRCh38
NC_000002.11:g.190428969C= , CM000664.1:g.190428969C= GRCh37
NC_000002.10:g.190137214C= NCBI36
NG_009027.1:g.21569G= , LRG_837:g.21569G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.761-18G= MANE Select ENSP00000261024.3:n.761-18G=
ENST00000261024.6:c.761-18G= ENSP00000261024.2:n.761-18G=
NM_014585.5:c.761-18G= , LRG_837t1:c.761-18G= NP_055400.1:n.761-18G=
XM_005246505.1:c.641-18G= XP_005246562.1:n.641-18G=
XM_005246505.2:c.641-18G= XP_005246562.1:n.641-18G=
XM_017003938.2:c.641-18G= XP_016859427.1:n.641-18G=
NM_014585.6:c.761-18G= MANE Select NP_055400.1:n.761-18G=
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