Canonical Allele Identifier: CA413656434
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74422044A>G , CM000685.2:g.74422044A>G GRCh38
NC_000023.10:g.73641879A>G , CM000685.1:g.73641879A>G GRCh37
NC_000023.9:g.73558604A>G NCBI36
NG_011641.1:g.5795A>G
NG_011641.2:g.5795A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.407A>G MANE Select ENSP00000465734.1:p.Asn136Ser
ENST00000636771.1:c.153A>G
ENST00000587091.5:c.407A>G ENSP00000465734.1:p.Asn136Ser
NM_006517.4:c.407A>G NP_006508.2:p.Asn136Ser
XM_005262294.1:c.407A>G XP_005262351.1:p.Asn136Ser
XM_011531015.1:c.407A>G XP_011529317.1:p.Asn136Ser
NM_006517.5:c.407A>G MANE Select NP_006508.2:p.Asn136Ser