Canonical Allele Identifier: CA632114157

Gene: SLC44A2

Linked Data

• dbSNP Id: rs1568450297
• gnomAD v2: 19-10742110-AC-A
• gnomAD v4: 19-10631434-AC-A
• MyVariant Identifiers: chr19:g.10742111del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10631435del , CM000681.2:g.10631435del	GRCh38
NC_000019.9:g.10742111del , CM000681.1:g.10742111del	GRCh37
NC_000019.8:g.10603111del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000335757.10:c.442-40del MANE Select	ENSP00000336888.4:n.442-40del
ENST00000335757.9:c.442-40del	ENSP00000336888.4:n.442-40del
ENST00000407327.8:c.436-40del	ENSP00000385135.3:n.436-40del
ENST00000586078.5:c.442-40del	ENSP00000466664.1:n.442-40del
ENST00000588409.1:c.246-3321del	ENSP00000468070.1:n.246-3321del
ENST00000588465.5:n.351-40del
ENST00000588688.5:c.283-40del	ENSP00000467552.1:n.283-40del
ENST00000590382.5:c.277-40del	ENSP00000468691.1:n.277-40del
ENST00000590857.5:c.-108-40del	ENSP00000465547.1:n.-108-40del
ENST00000592293.5:c.*239-40del	ENSP00000466612.1:n.*239-40del
NM_001145056.1:c.436-40del	NP_001138528.1:n.436-40del
NM_020428.3:c.442-40del	NP_065161.3:n.442-40del
XM_005259997.1:c.442-40del	XP_005260054.1:n.442-40del
XM_005259999.1:c.436-40del	XP_005260056.1:n.436-40del
NM_001363611.1:c.442-40del	NP_001350540.1:n.442-40del
XM_005259999.2:c.436-40del	XP_005260056.1:n.436-40del
NM_020428.4:c.442-40del MANE Select	NP_065161.3:n.442-40del
NM_001145056.2:c.436-40del	NP_001138528.1:n.436-40del
NM_001363611.2:c.442-40del	NP_001350540.1:n.442-40del