Canonical Allele Identifier: CA2245612361

Gene: SLC16A11

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7042164C= , CM000679.2:g.7042164C=	GRCh38
NC_000017.10:g.6945483C= , CM000679.1:g.6945483C=	GRCh37
NC_000017.9:g.6886207C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001370549.1:c.946G= MANE Select	NP_001357478.1:p.Gly316=
ENST00000574600.3:c.946G= MANE Select	ENSP00000460927.2:p.Gly316=
NM_001370553.1:c.946G=	NP_001357482.1:p.Gly316=
NM_153357.1:c.1018G=	NP_699188.1:p.Gly340=
NM_153357.2:c.946G=	NP_699188.2:p.Gly316=
NM_153357.3:c.946G=	NP_699188.2:p.Gly316=
ENST00000308009.5:c.1018G=	ENSP00000310490.1:p.Gly340=
ENST00000447225.1:c.922G=	ENSP00000394449.1:p.Gly308=
ENST00000573338.1:n.678-256G=
ENST00000662352.3:c.946G=	ENSP00000499634.1:p.Gly316=
ENST00000673828.2:c.946G=	ENSP00000501313.1:p.Gly316=
XM_005256488.2:c.1303G=	XP_005256545.2:p.Gly435=
XM_005256488.4:c.1303G=	XP_005256545.2:p.Gly435=
XM_017024281.1:c.1303G=	XP_016879770.1:p.Gly435=
XM_017024282.2:c.704-256G=	XP_016879771.1:n.704-256G=