Canonical Allele Identifier: CA349987671
Gene: SLC40A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.190428577C>G (hg19) chr2:g.189563851C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563851C>G , CM000664.2:g.189563851C>G GRCh38
NC_000002.11:g.190428577C>G , CM000664.1:g.190428577C>G GRCh37
NC_000002.10:g.190136822C>G NCBI36
NG_009027.1:g.21961G>C , LRG_837:g.21961G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261024.7:c.1135G>C MANE Select ENSP00000261024.3:p.Ala379Pro
ENST00000261024.6:c.1135G>C ENSP00000261024.2:p.Ala379Pro
NM_014585.5:c.1135G>C , LRG_837t1:c.1135G>C NP_055400.1:p.Ala379Pro
XM_005246505.1:c.1015G>C XP_005246562.1:p.Ala339Pro
XM_005246505.2:c.1015G>C XP_005246562.1:p.Ala339Pro
XM_017003938.2:c.1015G>C XP_016859427.1:p.Ala339Pro
NM_014585.6:c.1135G>C MANE Select NP_055400.1:p.Ala379Pro
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