Canonical Allele Identifier: CA2694114385

Gene: SLC16A2

Linked Data

• gnomAD v4: X-74422120-C-CGGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74422121_74422122insGGAG , CM000685.2:g.74422121_74422122insGGAG	GRCh38
NC_000023.10:g.73641956_73641957insGGAG , CM000685.1:g.73641956_73641957insGGAG	GRCh37
NC_000023.9:g.73558681_73558682insGGAG	NCBI36
NG_011641.1:g.5872_5873insGGAG
NG_011641.2:g.5872_5873insGGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.430+54_430+55insGGAG MANE Select	ENSP00000465734.1:n.430+54_430+55insGGAG
ENST00000636771.1:c.176+54_176+55insGGAG
ENST00000587091.5:c.430+54_430+55insGGAG	ENSP00000465734.1:n.430+54_430+55insGGAG
NM_006517.4:c.430+54_430+55insGGAG	NP_006508.2:n.430+54_430+55insGGAG
XM_005262294.1:c.430+54_430+55insGGAG	XP_005262351.1:n.430+54_430+55insGGAG
XM_011531015.1:c.430+54_430+55insGGAG	XP_011529317.1:n.430+54_430+55insGGAG
NM_006517.5:c.430+54_430+55insGGAG MANE Select	NP_006508.2:n.430+54_430+55insGGAG