Canonical Allele Identifier: CA505385824

Gene: SLC44A2

Linked Data

• MyVariant Identifiers: chr19:g.10741814C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10631138C>G , CM000681.2:g.10631138C>G	GRCh38
NC_000019.9:g.10741814C>G , CM000681.1:g.10741814C>G	GRCh37
NC_000019.8:g.10602814C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335757.10:c.327C>G MANE Select	ENSP00000336888.4:p.Pro109=
ENST00000335757.9:c.327C>G	ENSP00000336888.4:p.Pro109=
ENST00000407327.8:c.321C>G	ENSP00000385135.3:p.Pro107=
ENST00000586078.5:c.327C>G	ENSP00000466664.1:p.Pro109=
ENST00000588409.1:c.245+3134C>G	ENSP00000468070.1:n.245+3134C>G
ENST00000588465.5:n.236C>G
ENST00000588688.5:c.168C>G	ENSP00000467552.1:p.Pro56=
ENST00000590382.5:c.162C>G	ENSP00000468691.1:p.Pro54=
ENST00000590857.5:c.-223C>G	ENSP00000465547.1:n.-223C>G
ENST00000592293.5:c.*124C>G	ENSP00000466612.1:n.*124C>G
NM_001145056.1:c.321C>G	NP_001138528.1:p.Pro107=
NM_020428.3:c.327C>G	NP_065161.3:p.Pro109=
XM_005259997.1:c.327C>G	XP_005260054.1:p.Pro109=
XM_005259999.1:c.321C>G	XP_005260056.1:p.Pro107=
NM_001363611.1:c.327C>G	NP_001350540.1:p.Pro109=
XM_005259999.2:c.321C>G	XP_005260056.1:p.Pro107=
NM_020428.4:c.327C>G MANE Select	NP_065161.3:p.Pro109=
NM_001145056.2:c.321C>G	NP_001138528.1:p.Pro107=
NM_001363611.2:c.327C>G	NP_001350540.1:p.Pro109=