Canonical Allele Identifier: CA2792364805

Gene: SLC22A8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62995864_62995866del , CM000673.2:g.62995864_62995866del	GRCh38
NC_000011.9:g.62763336_62763338del , CM000673.1:g.62763336_62763338del	GRCh37
NC_000011.8:g.62519912_62519914del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.886-46_886-44del MANE Select	ENSP00000337335.2:n.886-46_886-44del
ENST00000311438.12:c.886-46_886-44del	ENSP00000311463.8:n.886-46_886-44del
ENST00000336232.6:c.886-46_886-44del	ENSP00000337335.2:n.886-46_886-44del
ENST00000430500.6:c.886-46_886-44del	ENSP00000398548.2:n.886-46_886-44del
ENST00000535878.5:c.517-46_517-44del	ENSP00000443368.1:n.517-46_517-44del
ENST00000539841.1:n.867_869del
ENST00000545207.5:c.613-46_613-44del	ENSP00000441658.1:n.613-46_613-44del
NM_001184732.1:c.886-46_886-44del	NP_001171661.1:n.886-46_886-44del
NM_001184733.1:c.613-46_613-44del	NP_001171662.1:n.613-46_613-44del
NM_001184736.1:c.517-46_517-44del	NP_001171665.1:n.517-46_517-44del
NM_004254.3:c.886-46_886-44del	NP_004245.2:n.886-46_886-44del
XM_011545364.1:c.517-46_517-44del	XP_011543666.1:n.517-46_517-44del
NM_004254.4:c.886-46_886-44del MANE Select	NP_004245.2:n.886-46_886-44del
NM_001184732.2:c.886-46_886-44del	NP_001171661.1:n.886-46_886-44del
NM_001184733.2:c.613-46_613-44del	NP_001171662.1:n.613-46_613-44del
NM_001184736.2:c.517-46_517-44del	NP_001171665.1:n.517-46_517-44del