Canonical Allele Identifier: CA2740352259

Gene: SLC40A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189565630_189565631insAGGGAACATTAACTCC , CM000664.2:g.189565630_189565631insAGGGAACATTAACTCC	GRCh38
NC_000002.11:g.190430356_190430357insAGGGAACATTAACTCC , CM000664.1:g.190430356_190430357insAGGGAACATTAACTCC	GRCh37
NC_000002.10:g.190138601_190138602insAGGGAACATTAACTCC	NCBI36
NG_009027.1:g.20181_20182insGGAGTTAATGTTCCCT , LRG_837:g.20181_20182insGGAGTTAATGTTCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.515-32_515-31insGGAGTTAATGTTCCCT MANE Select	ENSP00000261024.3:n.515-32_515-31insGGAGTTAATGTTCCCT
ENST00000261024.6:c.515-32_515-31insGGAGTTAATGTTCCCT	ENSP00000261024.2:n.515-32_515-31insGGAGTTAATGTTCCCT
ENST00000427241.5:c.515-32_515-31insGGAGTTAATGTTCCCT	ENSP00000390005.1:n.515-32_515-31insGGAGTTAATGTTCCCT
NM_014585.5:c.515-32_515-31insGGAGTTAATGTTCCCT , LRG_837t1:c.515-32_515-31insGGAGTTAATGTTCCCT	NP_055400.1:n.515-32_515-31insGGAGTTAATGTTCCCT
XM_005246505.1:c.395-32_395-31insGGAGTTAATGTTCCCT	XP_005246562.1:n.395-32_395-31insGGAGTTAATGTTCCCT
XM_005246505.2:c.395-32_395-31insGGAGTTAATGTTCCCT	XP_005246562.1:n.395-32_395-31insGGAGTTAATGTTCCCT
XM_017003938.2:c.395-32_395-31insGGAGTTAATGTTCCCT	XP_016859427.1:n.395-32_395-31insGGAGTTAATGTTCCCT
NM_014585.6:c.515-32_515-31insGGAGTTAATGTTCCCT MANE Select	NP_055400.1:n.515-32_515-31insGGAGTTAATGTTCCCT