Canonical Allele Identifier: CA2437472686

Gene: SLC16A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74422073_74422083delinsTGGCCCCGCAC , CM000685.2:g.74422073_74422083delinsTGGCCCCGCAC	GRCh38
NC_000023.10:g.73641908_73641918delinsTGGCCCCGCAC , CM000685.1:g.73641908_73641918delinsTGGCCCCGCAC	GRCh37
NC_000023.9:g.73558633_73558643delinsTGGCCCCGCAC	NCBI36
NG_011641.1:g.5824_5834delinsTGGCCCCGCAC
NG_011641.2:g.5824_5834delinsTGGCCCCGCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.430+6_430+16delinsTGGCCCCGCAC MANE Select	ENSP00000465734.1:n.430+6_430+16delinsTGGCCCCGCAC
ENST00000636771.1:c.176+6_176+16delinsTGGCCCCGCAC
ENST00000587091.5:c.430+6_430+16delinsTGGCCCCGCAC	ENSP00000465734.1:n.430+6_430+16delinsTGGCCCCGCAC
NM_006517.4:c.430+6_430+16delinsTGGCCCCGCAC	NP_006508.2:n.430+6_430+16delinsTGGCCCCGCAC
XM_005262294.1:c.430+6_430+16delinsTGGCCCCGCAC	XP_005262351.1:n.430+6_430+16delinsTGGCCCCGCAC
XM_011531015.1:c.430+6_430+16delinsTGGCCCCGCAC	XP_011529317.1:n.430+6_430+16delinsTGGCCCCGCAC
NM_006517.5:c.430+6_430+16delinsTGGCCCCGCAC MANE Select	NP_006508.2:n.430+6_430+16delinsTGGCCCCGCAC