Canonical Allele Identifier: CA2482726132
Gene: SLC41A1 HGNC NCBI

Linked Data

dbSNP Id: rs823156
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205795512G>C , CM000663.2:g.205795512G>C GRCh38
NC_000001.10:g.205764640G>C , CM000663.1:g.205764640G>C GRCh37
NC_000001.9:g.204031263G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367137.4:c.1073-34C>G MANE Select ENSP00000356105.3:n.1073-34C>G
ENST00000367137.3:c.1073-34C>G ENSP00000356105.3:n.1073-34C>G
ENST00000468057.5:n.869-34C>G
ENST00000484228.1:n.1105C>G
NM_173854.5:c.1073-34C>G NP_776253.3:n.1073-34C>G
XM_005245069.1:c.1073-34C>G XP_005245126.1:n.1073-34C>G
XM_005245069.2:c.1073-34C>G XP_005245126.1:n.1073-34C>G
NM_173854.6:c.1073-34C>G MANE Select NP_776253.3:n.1073-34C>G
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