Canonical Allele Identifier: CA1315653565

Gene: SLC40A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575150_189575151delinsAC , CM000664.2:g.189575150_189575151delinsAC	GRCh38
NC_000002.11:g.190439876_190439877delinsAC , CM000664.1:g.190439876_190439877delinsAC	GRCh37
NC_000002.10:g.190148121_190148122delinsAC	NCBI36
NG_009027.1:g.10661_10662delinsGT , LRG_837:g.10661_10662delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000261024.7:c.271+10_271+11delinsGT MANE Select	ENSP00000261024.3:n.271+10_271+11delinsGT
ENST00000261024.6:c.271+10_271+11delinsGT	ENSP00000261024.2:n.271+10_271+11delinsGT
ENST00000427241.5:c.271+10_271+11delinsGT	ENSP00000390005.1:n.271+10_271+11delinsGT
ENST00000479598.5:n.552+10_552+11delinsGT
NM_014585.5:c.271+10_271+11delinsGT , LRG_837t1:c.271+10_271+11delinsGT	NP_055400.1:n.271+10_271+11delinsGT
XM_005246505.1:c.151+10_151+11delinsGT	XP_005246562.1:n.151+10_151+11delinsGT
XM_005246505.2:c.151+10_151+11delinsGT	XP_005246562.1:n.151+10_151+11delinsGT
XM_017003938.2:c.151+10_151+11delinsGT	XP_016859427.1:n.151+10_151+11delinsGT
NM_014585.6:c.271+10_271+11delinsGT MANE Select	NP_055400.1:n.271+10_271+11delinsGT