Canonical Allele Identifier: CA9198354
Gene: SLC44A2 HGNC NCBI

Linked Data

dbSNP Id: rs2288904

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10631494A>G , CM000681.2:g.10631494A>G GRCh38
NC_000019.9:g.10742170A>G , CM000681.1:g.10742170A>G GRCh37
NC_000019.8:g.10603170A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000335757.10:c.461A>G MANE Select ENSP00000336888.4:p.Gln154Arg
ENST00000335757.9:c.461A>G ENSP00000336888.4:p.Gln154Arg
ENST00000407327.8:c.455A>G ENSP00000385135.3:p.Gln152Arg
ENST00000586078.5:c.461A>G ENSP00000466664.1:p.Gln154Arg
ENST00000588409.1:c.246-3262A>G ENSP00000468070.1:p.=
ENST00000588465.5:n.370A>G
ENST00000588688.5:c.302A>G ENSP00000467552.1:p.Gln101Arg
ENST00000590382.5:c.296A>G ENSP00000468691.1:p.Gln99Arg
ENST00000590857.5:c.-89A>G ENSP00000465547.1:p.=
ENST00000592293.5:c.*258A>G ENSP00000466612.1:p.=
NM_001145056.1:c.455A>G NP_001138528.1:p.Gln152Arg
NM_020428.3:c.461A>G NP_065161.3:p.Gln154Arg
XM_005259997.1:c.461A>G XP_005260054.1:p.Gln154Arg
XM_005259999.1:c.455A>G XP_005260056.1:p.Gln152Arg
NM_001363611.1:c.461A>G NP_001350540.1:p.Gln154Arg
XM_005259999.2:c.455A>G XP_005260056.1:p.Gln152Arg
NM_020428.4:c.461A>G MANE Select NP_065161.3:p.Gln154Arg
NM_001145056.2:c.455A>G NP_001138528.1:p.Gln152Arg
NM_001363611.2:c.461A>G NP_001350540.1:p.Gln154Arg