Canonical Allele Identifier: CA1315653416

Gene: SLC40A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575022T= , CM000664.2:g.189575022T=	GRCh38
NC_000002.11:g.190439748T= , CM000664.1:g.190439748T=	GRCh37
NC_000002.10:g.190147993T=	NCBI36
NG_009027.1:g.10790A= , LRG_837:g.10790A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261024.7:c.271+139A= MANE Select	ENSP00000261024.3:n.271+139A=
ENST00000261024.6:c.271+139A=	ENSP00000261024.2:n.271+139A=
ENST00000427241.5:c.271+139A=	ENSP00000390005.1:n.271+139A=
ENST00000479598.5:n.552+139A=
NM_014585.5:c.271+139A= , LRG_837t1:c.271+139A=	NP_055400.1:n.271+139A=
XM_005246505.1:c.151+139A=	XP_005246562.1:n.151+139A=
XM_005246505.2:c.151+139A=	XP_005246562.1:n.151+139A=
XM_017003938.2:c.151+139A=	XP_016859427.1:n.151+139A=
NM_014585.6:c.271+139A= MANE Select	NP_055400.1:n.271+139A=