Canonical Allele Identifier: CA2322525659

Gene: SLC44A2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10631297A= , CM000681.2:g.10631297A=	GRCh38
NC_000019.9:g.10741973A= , CM000681.1:g.10741973A=	GRCh37
NC_000019.8:g.10602973A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335757.10:c.353A= MANE Select	ENSP00000336888.4:p.Asp118=
ENST00000335757.9:c.353A=	ENSP00000336888.4:p.Asp118=
ENST00000407327.8:c.347A=	ENSP00000385135.3:p.Asp116=
ENST00000586078.5:c.353A=	ENSP00000466664.1:p.Asp118=
ENST00000588409.1:c.245+3293A=	ENSP00000468070.1:n.245+3293A=
ENST00000588465.5:n.262A=
ENST00000588688.5:c.194A=	ENSP00000467552.1:p.Asp65=
ENST00000590382.5:c.188A=	ENSP00000468691.1:p.Asp63=
ENST00000590857.5:c.-197A=	ENSP00000465547.1:n.-197A=
ENST00000592293.5:c.*150A=	ENSP00000466612.1:n.*150A=
NM_001145056.1:c.347A=	NP_001138528.1:p.Asp116=
NM_020428.3:c.353A=	NP_065161.3:p.Asp118=
XM_005259997.1:c.353A=	XP_005260054.1:p.Asp118=
XM_005259999.1:c.347A=	XP_005260056.1:p.Asp116=
NM_001363611.1:c.353A=	NP_001350540.1:p.Asp118=
XM_005259999.2:c.347A=	XP_005260056.1:p.Asp116=
NM_020428.4:c.353A= MANE Select	NP_065161.3:p.Asp118=
NM_001145056.2:c.347A=	NP_001138528.1:p.Asp116=
NM_001363611.2:c.353A=	NP_001350540.1:p.Asp118=