Canonical Allele Identifier: CA2322525760

Gene: SLC44A2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10631516C= , CM000681.2:g.10631516C=	GRCh38
NC_000019.9:g.10742192C= , CM000681.1:g.10742192C=	GRCh37
NC_000019.8:g.10603192C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335757.10:c.483C= MANE Select	ENSP00000336888.4:p.Val161=
ENST00000335757.9:c.483C=	ENSP00000336888.4:p.Val161=
ENST00000407327.8:c.477C=	ENSP00000385135.3:p.Val159=
ENST00000586078.5:c.483C=	ENSP00000466664.1:p.Val161=
ENST00000588409.1:c.246-3240C=	ENSP00000468070.1:n.246-3240C=
ENST00000588465.5:n.392C=
ENST00000588688.5:c.324C=	ENSP00000467552.1:p.Val108=
ENST00000590382.5:c.318C=	ENSP00000468691.1:p.Val106=
ENST00000590857.5:c.-67C=	ENSP00000465547.1:n.-67C=
ENST00000592293.5:c.*280C=	ENSP00000466612.1:n.*280C=
NM_001145056.1:c.477C=	NP_001138528.1:p.Val159=
NM_020428.3:c.483C=	NP_065161.3:p.Val161=
XM_005259997.1:c.483C=	XP_005260054.1:p.Val161=
XM_005259999.1:c.477C=	XP_005260056.1:p.Val159=
NM_001363611.1:c.483C=	NP_001350540.1:p.Val161=
XM_005259999.2:c.477C=	XP_005260056.1:p.Val159=
NM_020428.4:c.483C= MANE Select	NP_065161.3:p.Val161=
NM_001145056.2:c.477C=	NP_001138528.1:p.Val159=
NM_001363611.2:c.483C=	NP_001350540.1:p.Val161=