Canonical Allele Identifier: CA2245613272

Gene: SLC16A11

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7043011C= , CM000679.2:g.7043011C=	GRCh38
NC_000017.10:g.6946330C= , CM000679.1:g.6946330C=	GRCh37
NC_000017.9:g.6887054C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001370549.1:c.265G= MANE Select	NP_001357478.1:p.Val89=
ENST00000574600.3:c.265G= MANE Select	ENSP00000460927.2:p.Val89=
NM_001370553.1:c.265G=	NP_001357482.1:p.Val89=
NM_153357.1:c.337G=	NP_699188.1:p.Val113=
NM_153357.2:c.265G=	NP_699188.2:p.Val89=
NM_153357.3:c.265G=	NP_699188.2:p.Val89=
ENST00000308009.5:c.337G=	ENSP00000310490.1:p.Val113=
ENST00000447225.1:c.265G=	ENSP00000394449.1:p.Val89=
ENST00000573338.1:n.596G=
ENST00000574600.1:c.265G=	ENSP00000460927.1:p.Val89=
ENST00000662352.3:c.265G=	ENSP00000499634.1:p.Val89=
ENST00000673828.2:c.265G=	ENSP00000501313.1:p.Val89=
XM_005256488.2:c.622G=	XP_005256545.2:p.Val208=
XM_005256488.4:c.622G=	XP_005256545.2:p.Val208=
XM_011523696.1:c.622G=	XP_011521998.1:p.Val208=
XM_017024281.1:c.622G=	XP_016879770.1:p.Val208=
XM_017024282.2:c.622G=	XP_016879771.1:p.Val208=