Canonical Allele Identifier: CA2322525560

Gene: SLC44A2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10631093A= , CM000681.2:g.10631093A=	GRCh38
NC_000019.9:g.10741769A= , CM000681.1:g.10741769A=	GRCh37
NC_000019.8:g.10602769A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335757.10:c.282A= MANE Select	ENSP00000336888.4:p.Lys94=
ENST00000335757.9:c.282A=	ENSP00000336888.4:p.Lys94=
ENST00000407327.8:c.276A=	ENSP00000385135.3:p.Lys92=
ENST00000586078.5:c.282A=	ENSP00000466664.1:p.Lys94=
ENST00000588409.1:c.245+3089A=	ENSP00000468070.1:n.245+3089A=
ENST00000588465.5:n.191A=
ENST00000588688.5:c.123A=	ENSP00000467552.1:p.Lys41=
ENST00000590382.5:c.117A=	ENSP00000468691.1:p.Lys39=
ENST00000590857.5:c.-268A=	ENSP00000465547.1:n.-268A=
ENST00000592293.5:c.*79A=	ENSP00000466612.1:n.*79A=
NM_001145056.1:c.276A=	NP_001138528.1:p.Lys92=
NM_020428.3:c.282A=	NP_065161.3:p.Lys94=
XM_005259997.1:c.282A=	XP_005260054.1:p.Lys94=
XM_005259999.1:c.276A=	XP_005260056.1:p.Lys92=
NM_001363611.1:c.282A=	NP_001350540.1:p.Lys94=
XM_005259999.2:c.276A=	XP_005260056.1:p.Lys92=
NM_020428.4:c.282A= MANE Select	NP_065161.3:p.Lys94=
NM_001145056.2:c.276A=	NP_001138528.1:p.Lys92=
NM_001363611.2:c.282A=	NP_001350540.1:p.Lys94=