Canonical Allele Identifier: CA404019288

Gene: SLC44A2

Linked Data

• MyVariant Identifiers: chr19:g.10742161A>T (hg19) ; chr19:g.10631485A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10631485A>T , CM000681.2:g.10631485A>T	GRCh38
NC_000019.9:g.10742161A>T , CM000681.1:g.10742161A>T	GRCh37
NC_000019.8:g.10603161A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335757.10:c.452A>T MANE Select	ENSP00000336888.4:p.Glu151Val
ENST00000335757.9:c.452A>T	ENSP00000336888.4:p.Glu151Val
ENST00000407327.8:c.446A>T	ENSP00000385135.3:p.Glu149Val
ENST00000586078.5:c.452A>T	ENSP00000466664.1:p.Glu151Val
ENST00000588409.1:c.246-3271A>T	ENSP00000468070.1:n.246-3271A>T
ENST00000588465.5:n.361A>T
ENST00000588688.5:c.293A>T	ENSP00000467552.1:p.Glu98Val
ENST00000590382.5:c.287A>T	ENSP00000468691.1:p.Glu96Val
ENST00000590857.5:c.-98A>T	ENSP00000465547.1:n.-98A>T
ENST00000592293.5:c.*249A>T	ENSP00000466612.1:n.*249A>T
NM_001145056.1:c.446A>T	NP_001138528.1:p.Glu149Val
NM_020428.3:c.452A>T	NP_065161.3:p.Glu151Val
XM_005259997.1:c.452A>T	XP_005260054.1:p.Glu151Val
XM_005259999.1:c.446A>T	XP_005260056.1:p.Glu149Val
NM_001363611.1:c.452A>T	NP_001350540.1:p.Glu151Val
XM_005259999.2:c.446A>T	XP_005260056.1:p.Glu149Val
NM_020428.4:c.452A>T MANE Select	NP_065161.3:p.Glu151Val
NM_001145056.2:c.446A>T	NP_001138528.1:p.Glu149Val
NM_001363611.2:c.452A>T	NP_001350540.1:p.Glu151Val