Canonical Allele Identifier: CA2582408708
Gene: SLC44A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10631195C>A , CM000681.2:g.10631195C>A GRCh38
NC_000019.9:g.10741871C>A , CM000681.1:g.10741871C>A GRCh37
NC_000019.8:g.10602871C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000335757.10:c.330+54C>A MANE Select ENSP00000336888.4:n.330+54C>A
ENST00000335757.9:c.330+54C>A ENSP00000336888.4:n.330+54C>A
ENST00000407327.8:c.324+54C>A ENSP00000385135.3:n.324+54C>A
ENST00000586078.5:c.330+54C>A ENSP00000466664.1:n.330+54C>A
ENST00000588409.1:c.245+3191C>A ENSP00000468070.1:n.245+3191C>A
ENST00000588465.5:n.239+54C>A
ENST00000588688.5:c.171+54C>A ENSP00000467552.1:n.171+54C>A
ENST00000590382.5:c.165+54C>A ENSP00000468691.1:n.165+54C>A
ENST00000590857.5:c.-220+54C>A ENSP00000465547.1:n.-220+54C>A
ENST00000592293.5:c.*127+54C>A ENSP00000466612.1:n.*127+54C>A
NM_001145056.1:c.324+54C>A NP_001138528.1:n.324+54C>A
NM_020428.3:c.330+54C>A NP_065161.3:n.330+54C>A
XM_005259997.1:c.330+54C>A XP_005260054.1:n.330+54C>A
XM_005259999.1:c.324+54C>A XP_005260056.1:n.324+54C>A
NM_001363611.1:c.330+54C>A NP_001350540.1:n.330+54C>A
XM_005259999.2:c.324+54C>A XP_005260056.1:n.324+54C>A
NM_020428.4:c.330+54C>A MANE Select NP_065161.3:n.330+54C>A
NM_001145056.2:c.324+54C>A NP_001138528.1:n.324+54C>A
NM_001363611.2:c.330+54C>A NP_001350540.1:n.330+54C>A