Canonical Allele Identifier: CA2437510018
Gene: SLC16A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74531308G= , CM000685.2:g.74531308G= GRCh38
NC_000023.10:g.73751143G= , CM000685.1:g.73751143G= GRCh37
NC_000023.9:g.73667868G= NCBI36
NG_011641.1:g.115059G=
NG_011641.2:g.115059G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.1400-25G= MANE Select ENSP00000465734.1:n.1400-25G=
ENST00000636771.1:c.1309-25G=
ENST00000587091.5:c.1400-25G= ENSP00000465734.1:n.1400-25G=
ENST00000590447.1:c.611-25G=
NM_006517.4:c.1400-25G= NP_006508.2:n.1400-25G=
XM_005262294.1:c.1171-25G= XP_005262351.1:n.1171-25G=
NM_006517.5:c.1400-25G= MANE Select NP_006508.2:n.1400-25G=