Canonical Allele Identifier: CA8335109

Gene: SLC16A11

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7041768G>C , CM000679.2:g.7041768G>C	GRCh38
NC_000017.10:g.6945087G>C , CM000679.1:g.6945087G>C	GRCh37
NC_000017.9:g.6885811G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574600.3:c.1255C>G MANE Select	ENSP00000460927.2:p.Pro419Ala
ENST00000662352.3:c.1255C>G	ENSP00000499634.1:p.Pro419Ala
ENST00000673828.2:c.*163C>G	ENSP00000501313.1:n.*163C>G
ENST00000308009.5:c.1327C>G	ENSP00000310490.1:p.Pro443Ala
ENST00000447225.1:c.1231C>G	ENSP00000394449.1:p.Pro411Ala
ENST00000573338.1:n.818C>G
NM_153357.1:c.1327C>G	NP_699188.1:p.Pro443Ala
XM_005256488.2:c.1612C>G	XP_005256545.2:p.Pro538Ala
XM_005256488.4:c.1612C>G	XP_005256545.2:p.Pro538Ala
XM_017024282.2:c.844C>G	XP_016879771.1:p.Pro282Ala
NM_153357.2:c.1255C>G	NP_699188.2:p.Pro419Ala
NM_001370549.1:c.1255C>G MANE Select	NP_001357478.1:p.Pro419Ala
NM_001370553.1:c.*163C>G	NP_001357482.1:n.*163C>G
NM_153357.3:c.1255C>G	NP_699188.2:p.Pro419Ala