Canonical Allele Identifier: CA1189548214

Gene: SLC16A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.112913674_112913688delinsACTTCTTTCCCCCAT , CM000663.2:g.112913674_112913688delinsACTTCTTTCCCCCAT	GRCh38
NC_000001.10:g.113456296_113456310delinsACTTCTTTCCCCCAT , CM000663.1:g.113456296_113456310delinsACTTCTTTCCCCCAT	GRCh37
NC_000001.9:g.113257819_113257833delinsACTTCTTTCCCCCAT	NCBI36
NG_015880.2:g.47241_47255delinsATGGGGGAAAGAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369626.8:c.*203_*217delinsATGGGGGAAAGAAGT MANE Select	ENSP00000358640.4:n.*203_*217delinsATGGGGGAAAGAAGT
ENST00000429288.2:c.*203_*217delinsATGGGGGAAAGAAGT	ENSP00000397106.2:n.*203_*217delinsATGGGGGAAAGAAGT
ENST00000443580.6:c.*203_*217delinsATGGGGGAAAGAAGT	ENSP00000399104.2:n.*203_*217delinsATGGGGGAAAGAAGT
ENST00000458229.6:c.*203_*217delinsATGGGGGAAAGAAGT	ENSP00000416167.2:n.*203_*217delinsATGGGGGAAAGAAGT
ENST00000679803.1:c.*203_*217delinsATGGGGGAAAGAAGT	ENSP00000505879.1:n.*203_*217delinsATGGGGGAAAGAAGT
ENST00000369626.7:c.*203_*217delinsATGGGGGAAAGAAGT	ENSP00000358640.3:n.*203_*217delinsATGGGGGAAAGAAGT
ENST00000538576.5:c.*203_*217delinsATGGGGGAAAGAAGT	ENSP00000441065.1:n.*203_*217delinsATGGGGGAAAGAAGT
NM_001166496.1:c.*203_*217delinsATGGGGGAAAGAAGT	NP_001159968.1:n.*203_*217delinsATGGGGGAAAGAAGT
NM_003051.3:c.*203_*217delinsATGGGGGAAAGAAGT	NP_003042.3:n.*203_*217delinsATGGGGGAAAGAAGT
XM_011542026.1:c.*203_*217delinsATGGGGGAAAGAAGT	XP_011540328.1:n.*203_*217delinsATGGGGGAAAGAAGT
XM_011542027.1:c.*203_*217delinsATGGGGGAAAGAAGT	XP_011540329.1:n.*203_*217delinsATGGGGGAAAGAAGT
NM_003051.4:c.*203_*217delinsATGGGGGAAAGAAGT MANE Select	NP_003042.3:n.*203_*217delinsATGGGGGAAAGAAGT
NM_001166496.2:c.*203_*217delinsATGGGGGAAAGAAGT	NP_001159968.1:n.*203_*217delinsATGGGGGAAAGAAGT