Canonical Allele Identifier: CA505385750

Gene: SLC44A2

Linked Data

• MyVariant Identifiers: chr19:g.10741782C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10631106C>T , CM000681.2:g.10631106C>T	GRCh38
NC_000019.9:g.10741782C>T , CM000681.1:g.10741782C>T	GRCh37
NC_000019.8:g.10602782C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335757.10:c.295C>T MANE Select	ENSP00000336888.4:p.Leu99=
ENST00000335757.9:c.295C>T	ENSP00000336888.4:p.Leu99=
ENST00000407327.8:c.289C>T	ENSP00000385135.3:p.Leu97=
ENST00000586078.5:c.295C>T	ENSP00000466664.1:p.Leu99=
ENST00000588409.1:c.245+3102C>T	ENSP00000468070.1:n.245+3102C>T
ENST00000588465.5:n.204C>T
ENST00000588688.5:c.136C>T	ENSP00000467552.1:p.Leu46=
ENST00000590382.5:c.130C>T	ENSP00000468691.1:p.Leu44=
ENST00000590857.5:c.-255C>T	ENSP00000465547.1:n.-255C>T
ENST00000592293.5:c.*92C>T	ENSP00000466612.1:n.*92C>T
NM_001145056.1:c.289C>T	NP_001138528.1:p.Leu97=
NM_020428.3:c.295C>T	NP_065161.3:p.Leu99=
XM_005259997.1:c.295C>T	XP_005260054.1:p.Leu99=
XM_005259999.1:c.289C>T	XP_005260056.1:p.Leu97=
NM_001363611.1:c.295C>T	NP_001350540.1:p.Leu99=
XM_005259999.2:c.289C>T	XP_005260056.1:p.Leu97=
NM_020428.4:c.295C>T MANE Select	NP_065161.3:p.Leu99=
NM_001145056.2:c.289C>T	NP_001138528.1:p.Leu97=
NM_001363611.2:c.295C>T	NP_001350540.1:p.Leu99=