Canonical Allele Identifier: CA2322525559
Gene: SLC44A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10631092A= , CM000681.2:g.10631092A= GRCh38
NC_000019.9:g.10741768A= , CM000681.1:g.10741768A= GRCh37
NC_000019.8:g.10602768A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000335757.10:c.281A= MANE Select ENSP00000336888.4:p.Lys94=
ENST00000335757.9:c.281A= ENSP00000336888.4:p.Lys94=
ENST00000407327.8:c.275A= ENSP00000385135.3:p.Lys92=
ENST00000586078.5:c.281A= ENSP00000466664.1:p.Lys94=
ENST00000588409.1:c.245+3088A= ENSP00000468070.1:n.245+3088A=
ENST00000588465.5:n.190A=
ENST00000588688.5:c.122A= ENSP00000467552.1:p.Lys41=
ENST00000590382.5:c.116A= ENSP00000468691.1:p.Lys39=
ENST00000590857.5:c.-269A= ENSP00000465547.1:n.-269A=
ENST00000592293.5:c.*78A= ENSP00000466612.1:n.*78A=
NM_001145056.1:c.275A= NP_001138528.1:p.Lys92=
NM_020428.3:c.281A= NP_065161.3:p.Lys94=
XM_005259997.1:c.281A= XP_005260054.1:p.Lys94=
XM_005259999.1:c.275A= XP_005260056.1:p.Lys92=
NM_001363611.1:c.281A= NP_001350540.1:p.Lys94=
XM_005259999.2:c.275A= XP_005260056.1:p.Lys92=
NM_020428.4:c.281A= MANE Select NP_065161.3:p.Lys94=
NM_001145056.2:c.275A= NP_001138528.1:p.Lys92=
NM_001363611.2:c.281A= NP_001350540.1:p.Lys94=