Canonical Allele Identifier: CA919164787

Gene: SLC41A2

Linked Data

• dbSNP Id: rs1592935977

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.104821342_104821358del , CM000674.2:g.104821342_104821358del	GRCh38
NC_000012.11:g.105215120_105215136del , CM000674.1:g.105215120_105215136del	GRCh37
NC_000012.10:g.103739250_103739266del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258538.8:c.1537-16019_1537-16003del MANE Select	ENSP00000258538.3:n.1537-16019_1537-16003del
ENST00000258538.7:c.1537-16019_1537-16003del	ENSP00000258538.3:n.1537-16019_1537-16003del
ENST00000549713.1:n.89+12735_89+12751del
NM_032148.3:c.1537-16019_1537-16003del	NP_115524.3:n.1537-16019_1537-16003del
XM_005269176.1:c.1537-16019_1537-16003del	XP_005269233.1:n.1537-16019_1537-16003del
XM_005269178.1:c.1537-16019_1537-16003del	XP_005269235.1:n.1537-16019_1537-16003del
XM_005269179.1:c.1537-16019_1537-16003del	XP_005269236.1:n.1537-16019_1537-16003del
XM_006719630.2:c.1537-16019_1537-16003del	XP_006719693.1:n.1537-16019_1537-16003del
XM_011538807.1:c.1537-16019_1537-16003del	XP_011537109.1:n.1537-16019_1537-16003del
XM_011538808.1:c.1537-16019_1537-16003del	XP_011537110.1:n.1537-16019_1537-16003del
XM_011538809.1:c.1537-16019_1537-16003del	XP_011537111.1:n.1537-16019_1537-16003del
XM_011538810.1:c.1537-16019_1537-16003del	XP_011537112.1:n.1537-16019_1537-16003del
XM_011538811.1:c.1537-16019_1537-16003del	XP_011537113.1:n.1537-16019_1537-16003del
XM_011538812.1:c.*43+12735_*43+12751del	XP_011537114.1:n.*43+12735_*43+12751del
XM_011538813.1:c.859-16019_859-16003del	XP_011537115.1:n.859-16019_859-16003del
NM_001352169.1:c.1537-16019_1537-16003del	NP_001339098.1:n.1537-16019_1537-16003del
NM_001352170.1:c.1537-16019_1537-16003del	NP_001339099.1:n.1537-16019_1537-16003del
NM_001352171.1:c.1537-16019_1537-16003del	NP_001339100.1:n.1537-16019_1537-16003del
NM_001352172.1:c.1537-16019_1537-16003del	NP_001339101.1:n.1537-16019_1537-16003del
NM_032148.4:c.1537-16019_1537-16003del	NP_115524.3:n.1537-16019_1537-16003del
XM_011538810.2:c.1537-16019_1537-16003del	XP_011537112.1:n.1537-16019_1537-16003del
XM_011538811.2:c.1537-16019_1537-16003del	XP_011537113.1:n.1537-16019_1537-16003del
XM_011538813.2:c.859-16019_859-16003del	XP_011537115.1:n.859-16019_859-16003del
XM_017020013.1:c.1537-16019_1537-16003del	XP_016875502.1:n.1537-16019_1537-16003del
XM_017020014.1:c.*43+12735_*43+12751del	XP_016875503.1:n.*43+12735_*43+12751del
XM_017020016.2:c.904-16019_904-16003del	XP_016875505.1:n.904-16019_904-16003del
XM_017020017.1:c.901-16019_901-16003del	XP_016875506.1:n.901-16019_901-16003del
XM_024449219.1:c.1537-16019_1537-16003del	XP_024304987.1:n.1537-16019_1537-16003del
NM_001352170.2:c.1537-16019_1537-16003del	NP_001339099.1:n.1537-16019_1537-16003del
NM_001352171.2:c.1537-16019_1537-16003del	NP_001339100.1:n.1537-16019_1537-16003del
NM_001352172.2:c.1537-16019_1537-16003del	NP_001339101.1:n.1537-16019_1537-16003del
NM_032148.5:c.1537-16019_1537-16003del	NP_115524.3:n.1537-16019_1537-16003del
NM_001352169.2:c.1537-16019_1537-16003del	NP_001339098.1:n.1537-16019_1537-16003del
NM_001352170.3:c.1537-16019_1537-16003del	NP_001339099.1:n.1537-16019_1537-16003del
NM_001352171.3:c.1537-16019_1537-16003del MANE Select	NP_001339100.1:n.1537-16019_1537-16003del
NM_001352172.3:c.1537-16019_1537-16003del	NP_001339101.1:n.1537-16019_1537-16003del
NM_001387125.1:c.1537-16019_1537-16003del	NP_001374054.1:n.1537-16019_1537-16003del
NM_001387126.1:c.1537-16019_1537-16003del	NP_001374055.1:n.1537-16019_1537-16003del
NM_001387127.1:c.1537-16019_1537-16003del	NP_001374056.1:n.1537-16019_1537-16003del
NM_001387128.1:c.*43+12735_*43+12751del	NP_001374057.1:n.*43+12735_*43+12751del
NM_001387129.1:c.*43+12735_*43+12751del	NP_001374058.1:n.*43+12735_*43+12751del
NM_001387130.1:c.*43+12735_*43+12751del	NP_001374059.1:n.*43+12735_*43+12751del
NM_032148.6:c.1537-16019_1537-16003del	NP_115524.3:n.1537-16019_1537-16003del