Canonical Allele Identifier: CA1315650261

Gene: SLC40A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189571684_189571689delinsCTCATT , CM000664.2:g.189571684_189571689delinsCTCATT	GRCh38
NC_000002.11:g.190436410_190436415delinsCTCATT , CM000664.1:g.190436410_190436415delinsCTCATT	GRCh37
NC_000002.10:g.190144655_190144660delinsCTCATT	NCBI36
NG_009027.1:g.14123_14128delinsAATGAG , LRG_837:g.14123_14128delinsAATGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.514+26_514+31delinsAATGAG MANE Select	ENSP00000261024.3:n.514+26_514+31delinsAATGAG
ENST00000261024.6:c.514+26_514+31delinsAATGAG	ENSP00000261024.2:n.514+26_514+31delinsAATGAG
ENST00000427241.5:c.514+26_514+31delinsAATGAG	ENSP00000390005.1:n.514+26_514+31delinsAATGAG
NM_014585.5:c.514+26_514+31delinsAATGAG , LRG_837t1:c.514+26_514+31delinsAATGAG	NP_055400.1:n.514+26_514+31delinsAATGAG
XM_005246505.1:c.394+26_394+31delinsAATGAG	XP_005246562.1:n.394+26_394+31delinsAATGAG
XM_005246505.2:c.394+26_394+31delinsAATGAG	XP_005246562.1:n.394+26_394+31delinsAATGAG
XM_017003938.2:c.394+26_394+31delinsAATGAG	XP_016859427.1:n.394+26_394+31delinsAATGAG
NM_014585.6:c.514+26_514+31delinsAATGAG MANE Select	NP_055400.1:n.514+26_514+31delinsAATGAG