Canonical Allele Identifier: CA349989757
Gene: SLC40A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.190439968A>C (hg19) chr2:g.189575242A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575242A>C , CM000664.2:g.189575242A>C GRCh38
NC_000002.11:g.190439968A>C , CM000664.1:g.190439968A>C GRCh37
NC_000002.10:g.190148213A>C NCBI36
NG_009027.1:g.10570T>G , LRG_837:g.10570T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.190T>G MANE Select ENSP00000261024.3:p.Tyr64Asp
ENST00000261024.6:c.190T>G ENSP00000261024.2:p.Tyr64Asp
ENST00000418714.1:n.631T>G
ENST00000427241.5:c.190T>G ENSP00000390005.1:p.Tyr64Asp
ENST00000479598.5:n.471T>G
NM_014585.5:c.190T>G , LRG_837t1:c.190T>G NP_055400.1:p.Tyr64Asp
XM_005246505.1:c.70T>G XP_005246562.1:p.Tyr24Asp
XM_005246505.2:c.70T>G XP_005246562.1:p.Tyr24Asp
XM_017003938.2:c.70T>G XP_016859427.1:p.Tyr24Asp
NM_014585.6:c.190T>G MANE Select NP_055400.1:p.Tyr64Asp
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