Canonical Allele Identifier: CA2322525558

Gene: SLC44A2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10631088G= , CM000681.2:g.10631088G=	GRCh38
NC_000019.9:g.10741764G= , CM000681.1:g.10741764G=	GRCh37
NC_000019.8:g.10602764G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335757.10:c.277G= MANE Select	ENSP00000336888.4:p.Val93=
ENST00000335757.9:c.277G=	ENSP00000336888.4:p.Val93=
ENST00000407327.8:c.271G=	ENSP00000385135.3:p.Val91=
ENST00000586078.5:c.277G=	ENSP00000466664.1:p.Val93=
ENST00000588409.1:c.245+3084G=	ENSP00000468070.1:n.245+3084G=
ENST00000588465.5:n.186G=
ENST00000588688.5:c.118G=	ENSP00000467552.1:p.Val40=
ENST00000590382.5:c.112G=	ENSP00000468691.1:p.Val38=
ENST00000590857.5:c.-273G=	ENSP00000465547.1:n.-273G=
ENST00000592293.5:c.*74G=	ENSP00000466612.1:n.*74G=
NM_001145056.1:c.271G=	NP_001138528.1:p.Val91=
NM_020428.3:c.277G=	NP_065161.3:p.Val93=
XM_005259997.1:c.277G=	XP_005260054.1:p.Val93=
XM_005259999.1:c.271G=	XP_005260056.1:p.Val91=
NM_001363611.1:c.277G=	NP_001350540.1:p.Val93=
XM_005259999.2:c.271G=	XP_005260056.1:p.Val91=
NM_020428.4:c.277G= MANE Select	NP_065161.3:p.Val93=
NM_001145056.2:c.271G=	NP_001138528.1:p.Val91=
NM_001363611.2:c.277G=	NP_001350540.1:p.Val93=