Canonical Allele Identifier: CA1315653551

Gene: SLC40A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575148_189575149delinsTA , CM000664.2:g.189575148_189575149delinsTA	GRCh38
NC_000002.11:g.190439874_190439875delinsTA , CM000664.1:g.190439874_190439875delinsTA	GRCh37
NC_000002.10:g.190148119_190148120delinsTA	NCBI36
NG_009027.1:g.10663_10664delinsTA , LRG_837:g.10663_10664delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000261024.7:c.271+12_271+13delinsTA MANE Select	ENSP00000261024.3:n.271+12_271+13delinsTA
ENST00000261024.6:c.271+12_271+13delinsTA	ENSP00000261024.2:n.271+12_271+13delinsTA
ENST00000427241.5:c.271+12_271+13delinsTA	ENSP00000390005.1:n.271+12_271+13delinsTA
ENST00000479598.5:n.552+12_552+13delinsTA
NM_014585.5:c.271+12_271+13delinsTA , LRG_837t1:c.271+12_271+13delinsTA	NP_055400.1:n.271+12_271+13delinsTA
XM_005246505.1:c.151+12_151+13delinsTA	XP_005246562.1:n.151+12_151+13delinsTA
XM_005246505.2:c.151+12_151+13delinsTA	XP_005246562.1:n.151+12_151+13delinsTA
XM_017003938.2:c.151+12_151+13delinsTA	XP_016859427.1:n.151+12_151+13delinsTA
NM_014585.6:c.271+12_271+13delinsTA MANE Select	NP_055400.1:n.271+12_271+13delinsTA