Canonical Allele Identifier: CA505480847

Gene: SLC44A2

Linked Data

• MyVariant Identifiers: chr19:g.10742156G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10631480G>T , CM000681.2:g.10631480G>T	GRCh38
NC_000019.9:g.10742156G>T , CM000681.1:g.10742156G>T	GRCh37
NC_000019.8:g.10603156G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335757.10:c.447G>T MANE Select	ENSP00000336888.4:p.Val149=
ENST00000335757.9:c.447G>T	ENSP00000336888.4:p.Val149=
ENST00000407327.8:c.441G>T	ENSP00000385135.3:p.Val147=
ENST00000586078.5:c.447G>T	ENSP00000466664.1:p.Val149=
ENST00000588409.1:c.246-3276G>T	ENSP00000468070.1:n.246-3276G>T
ENST00000588465.5:n.356G>T
ENST00000588688.5:c.288G>T	ENSP00000467552.1:p.Val96=
ENST00000590382.5:c.282G>T	ENSP00000468691.1:p.Val94=
ENST00000590857.5:c.-103G>T	ENSP00000465547.1:n.-103G>T
ENST00000592293.5:c.*244G>T	ENSP00000466612.1:n.*244G>T
NM_001145056.1:c.441G>T	NP_001138528.1:p.Val147=
NM_020428.3:c.447G>T	NP_065161.3:p.Val149=
XM_005259997.1:c.447G>T	XP_005260054.1:p.Val149=
XM_005259999.1:c.441G>T	XP_005260056.1:p.Val147=
NM_001363611.1:c.447G>T	NP_001350540.1:p.Val149=
XM_005259999.2:c.441G>T	XP_005260056.1:p.Val147=
NM_020428.4:c.447G>T MANE Select	NP_065161.3:p.Val149=
NM_001145056.2:c.441G>T	NP_001138528.1:p.Val147=
NM_001363611.2:c.447G>T	NP_001350540.1:p.Val149=