Canonical Allele Identifier: CA2662329020
Gene: SLC40A1 HGNC NCBI

Linked Data

gnomAD v4: 2-189575029-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575029C>A , CM000664.2:g.189575029C>A GRCh38
NC_000002.11:g.190439755C>A , CM000664.1:g.190439755C>A GRCh37
NC_000002.10:g.190148000C>A NCBI36
NG_009027.1:g.10783G>T , LRG_837:g.10783G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261024.7:c.271+132G>T MANE Select ENSP00000261024.3:n.271+132G>T
ENST00000261024.6:c.271+132G>T ENSP00000261024.2:n.271+132G>T
ENST00000427241.5:c.271+132G>T ENSP00000390005.1:n.271+132G>T
ENST00000479598.5:n.552+132G>T
NM_014585.5:c.271+132G>T , LRG_837t1:c.271+132G>T NP_055400.1:n.271+132G>T
XM_005246505.1:c.151+132G>T XP_005246562.1:n.151+132G>T
XM_005246505.2:c.151+132G>T XP_005246562.1:n.151+132G>T
XM_017003938.2:c.151+132G>T XP_016859427.1:n.151+132G>T
NM_014585.6:c.271+132G>T MANE Select NP_055400.1:n.271+132G>T
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