Canonical Allele Identifier: CA1315653829

Gene: SLC40A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575347_189575348delinsAT , CM000664.2:g.189575347_189575348delinsAT	GRCh38
NC_000002.11:g.190440073_190440074delinsAT , CM000664.1:g.190440073_190440074delinsAT	GRCh37
NC_000002.10:g.190148318_190148319delinsAT	NCBI36
NG_009027.1:g.10464_10465delinsAT , LRG_837:g.10464_10465delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.112-28_112-27delinsAT MANE Select	ENSP00000261024.3:n.112-28_112-27delinsAT
ENST00000261024.6:c.112-28_112-27delinsAT	ENSP00000261024.2:n.112-28_112-27delinsAT
ENST00000418714.1:n.553-28_553-27delinsAT
ENST00000427241.5:c.112-28_112-27delinsAT	ENSP00000390005.1:n.112-28_112-27delinsAT
ENST00000455320.5:c.112-28_112-27delinsAT	ENSP00000413549.1:n.112-28_112-27delinsAT
ENST00000479598.5:n.393-28_393-27delinsAT
NM_014585.5:c.112-28_112-27delinsAT , LRG_837t1:c.112-28_112-27delinsAT	NP_055400.1:n.112-28_112-27delinsAT
XM_005246505.1:c.-9-28_-9-27delinsAT	XP_005246562.1:n.-9-28_-9-27delinsAT
XM_005246505.2:c.-9-28_-9-27delinsAT	XP_005246562.1:n.-9-28_-9-27delinsAT
XM_017003938.2:c.-9-28_-9-27delinsAT	XP_016859427.1:n.-9-28_-9-27delinsAT
NM_014585.6:c.112-28_112-27delinsAT MANE Select	NP_055400.1:n.112-28_112-27delinsAT