Canonical Allele Identifier: CA2245613231

Gene: SLC16A11

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7042968T= , CM000679.2:g.7042968T=	GRCh38
NC_000017.10:g.6946287T= , CM000679.1:g.6946287T=	GRCh37
NC_000017.9:g.6887011T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001370549.1:c.308A= MANE Select	NP_001357478.1:p.Asp103=
ENST00000574600.3:c.308A= MANE Select	ENSP00000460927.2:p.Asp103=
NM_001370553.1:c.308A=	NP_001357482.1:p.Asp103=
NM_153357.1:c.380A=	NP_699188.1:p.Asp127=
NM_153357.2:c.308A=	NP_699188.2:p.Asp103=
NM_153357.3:c.308A=	NP_699188.2:p.Asp103=
ENST00000308009.5:c.380A=	ENSP00000310490.1:p.Asp127=
ENST00000447225.1:c.308A=	ENSP00000394449.1:p.Asp103=
ENST00000573338.1:n.639A=
ENST00000662352.3:c.308A=	ENSP00000499634.1:p.Asp103=
ENST00000673828.2:c.308A=	ENSP00000501313.1:p.Asp103=
XM_005256488.2:c.665A=	XP_005256545.2:p.Asp222=
XM_005256488.4:c.665A=	XP_005256545.2:p.Asp222=
XM_011523696.1:c.665A=	XP_011521998.1:p.Asp222=
XM_017024281.1:c.665A=	XP_016879770.1:p.Asp222=
XM_017024282.2:c.665A=	XP_016879771.1:p.Asp222=