Canonical Allele Identifier: CA1315653553

Gene: SLC40A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575148_189575151delinsTAAC , CM000664.2:g.189575148_189575151delinsTAAC	GRCh38
NC_000002.11:g.190439874_190439877delinsTAAC , CM000664.1:g.190439874_190439877delinsTAAC	GRCh37
NC_000002.10:g.190148119_190148122delinsTAAC	NCBI36
NG_009027.1:g.10661_10664delinsGTTA , LRG_837:g.10661_10664delinsGTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.271+10_271+13delinsGTTA MANE Select	ENSP00000261024.3:n.271+10_271+13delinsGTTA
ENST00000261024.6:c.271+10_271+13delinsGTTA	ENSP00000261024.2:n.271+10_271+13delinsGTTA
ENST00000427241.5:c.271+10_271+13delinsGTTA	ENSP00000390005.1:n.271+10_271+13delinsGTTA
ENST00000479598.5:n.552+10_552+13delinsGTTA
NM_014585.5:c.271+10_271+13delinsGTTA , LRG_837t1:c.271+10_271+13delinsGTTA	NP_055400.1:n.271+10_271+13delinsGTTA
XM_005246505.1:c.151+10_151+13delinsGTTA	XP_005246562.1:n.151+10_151+13delinsGTTA
XM_005246505.2:c.151+10_151+13delinsGTTA	XP_005246562.1:n.151+10_151+13delinsGTTA
XM_017003938.2:c.151+10_151+13delinsGTTA	XP_016859427.1:n.151+10_151+13delinsGTTA
NM_014585.6:c.271+10_271+13delinsGTTA MANE Select	NP_055400.1:n.271+10_271+13delinsGTTA