Canonical Allele Identifier: CA2701181533

Gene: SLC40A1

Linked Data

• dbSNP Id: rs2105620632

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189564229_189564230insG , CM000664.2:g.189564229_189564230insG	GRCh38
NC_000002.11:g.190428955_190428956insG , CM000664.1:g.190428955_190428956insG	GRCh37
NC_000002.10:g.190137200_190137201insG	NCBI36
NG_009027.1:g.21582_21583insC , LRG_837:g.21582_21583insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.761-5_761-4insC MANE Select	ENSP00000261024.3:n.761-5_761-4insC
ENST00000261024.6:c.761-5_761-4insC	ENSP00000261024.2:n.761-5_761-4insC
NM_014585.5:c.761-5_761-4insC , LRG_837t1:c.761-5_761-4insC	NP_055400.1:n.761-5_761-4insC
XM_005246505.1:c.641-5_641-4insC	XP_005246562.1:n.641-5_641-4insC
XM_005246505.2:c.641-5_641-4insC	XP_005246562.1:n.641-5_641-4insC
XM_017003938.2:c.641-5_641-4insC	XP_016859427.1:n.641-5_641-4insC
NM_014585.6:c.761-5_761-4insC MANE Select	NP_055400.1:n.761-5_761-4insC