Canonical Allele Identifier: CA2322525693

Gene: SLC44A2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10631369G= , CM000681.2:g.10631369G=	GRCh38
NC_000019.9:g.10742045G= , CM000681.1:g.10742045G=	GRCh37
NC_000019.8:g.10603045G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335757.10:c.425G= MANE Select	ENSP00000336888.4:p.Gly142=
ENST00000335757.9:c.425G=	ENSP00000336888.4:p.Gly142=
ENST00000407327.8:c.419G=	ENSP00000385135.3:p.Gly140=
ENST00000586078.5:c.425G=	ENSP00000466664.1:p.Gly142=
ENST00000588409.1:c.245+3365G=	ENSP00000468070.1:n.245+3365G=
ENST00000588465.5:n.334G=
ENST00000588688.5:c.266G=	ENSP00000467552.1:p.Gly89=
ENST00000590382.5:c.260G=	ENSP00000468691.1:p.Gly87=
ENST00000590857.5:c.-125G=	ENSP00000465547.1:n.-125G=
ENST00000592293.5:c.*222G=	ENSP00000466612.1:n.*222G=
NM_001145056.1:c.419G=	NP_001138528.1:p.Gly140=
NM_020428.3:c.425G=	NP_065161.3:p.Gly142=
XM_005259997.1:c.425G=	XP_005260054.1:p.Gly142=
XM_005259999.1:c.419G=	XP_005260056.1:p.Gly140=
NM_001363611.1:c.425G=	NP_001350540.1:p.Gly142=
XM_005259999.2:c.419G=	XP_005260056.1:p.Gly140=
NM_020428.4:c.425G= MANE Select	NP_065161.3:p.Gly142=
NM_001145056.2:c.419G=	NP_001138528.1:p.Gly140=
NM_001363611.2:c.425G=	NP_001350540.1:p.Gly142=