Canonical Allele Identifier: CA413659006
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74531416T>C , CM000685.2:g.74531416T>C GRCh38
NC_000023.10:g.73751251T>C , CM000685.1:g.73751251T>C GRCh37
NC_000023.9:g.73667976T>C NCBI36
NG_011641.1:g.115167T>C
NG_011641.2:g.115167T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.1483T>C MANE Select ENSP00000465734.1:p.Phe495Leu
ENST00000636771.1:c.1392T>C
ENST00000587091.5:c.1483T>C ENSP00000465734.1:p.Phe495Leu
ENST00000590447.1:c.694T>C
NM_006517.4:c.1483T>C NP_006508.2:p.Phe495Leu
XM_005262294.1:c.*6T>C XP_005262351.1:n.*6T>C
NM_006517.5:c.1483T>C MANE Select NP_006508.2:p.Phe495Leu