Canonical Allele Identifier: CA397791435

Gene: SLC16A11

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7042358C>G , CM000679.2:g.7042358C>G	GRCh38
NC_000017.10:g.6945677C>G , CM000679.1:g.6945677C>G	GRCh37
NC_000017.9:g.6886401C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574600.3:c.752G>C MANE Select	ENSP00000460927.2:p.Gly251Ala
ENST00000662352.3:c.752G>C	ENSP00000499634.1:p.Gly251Ala
ENST00000673828.2:c.752G>C	ENSP00000501313.1:p.Gly251Ala
ENST00000308009.5:c.824G>C	ENSP00000310490.1:p.Gly275Ala
ENST00000447225.1:c.752G>C	ENSP00000394449.1:p.Gly251Ala
ENST00000573338.1:n.678-450G>C
NM_153357.1:c.824G>C	NP_699188.1:p.Gly275Ala
XM_005256488.2:c.1109G>C	XP_005256545.2:p.Gly370Ala
XM_005256488.4:c.1109G>C	XP_005256545.2:p.Gly370Ala
XM_017024281.1:c.1109G>C	XP_016879770.1:p.Gly370Ala
XM_017024282.2:c.704-450G>C	XP_016879771.1:n.704-450G>C
NM_153357.2:c.752G>C	NP_699188.2:p.Gly251Ala
NM_001370549.1:c.752G>C MANE Select	NP_001357478.1:p.Gly251Ala
NM_001370553.1:c.752G>C	NP_001357482.1:p.Gly251Ala
NM_153357.3:c.752G>C	NP_699188.2:p.Gly251Ala