Canonical Allele Identifier: CA2579647158

Gene: SLC16A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74525667G>T , CM000685.2:g.74525667G>T	GRCh38
NC_000023.10:g.73745502G>T , CM000685.1:g.73745502G>T	GRCh37
NC_000023.9:g.73662227G>T	NCBI36
NG_011641.1:g.109418G>T
NG_011641.2:g.109418G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000587091.6:c.1027-83G>T MANE Select	ENSP00000465734.1:n.1027-83G>T
ENST00000636771.1:c.936-83G>T
ENST00000587091.5:c.1027-83G>T	ENSP00000465734.1:n.1027-83G>T
ENST00000590447.1:c.467-83G>T
NM_006517.4:c.1027-83G>T	NP_006508.2:n.1027-83G>T
XM_005262294.1:c.1027-83G>T	XP_005262351.1:n.1027-83G>T
XM_011531015.1:c.*31-83G>T	XP_011529317.1:n.*31-83G>T
NM_006517.5:c.1027-83G>T MANE Select	NP_006508.2:n.1027-83G>T