Canonical Allele Identifier: CA10650096

Gene: SLC25A19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75289395_75289398del , CM000679.2:g.75289395_75289398del	GRCh38
NC_000017.10:g.73285476_73285479del , CM000679.1:g.73285476_73285479del	GRCh37
NC_000017.9:g.70797071_70797074del	NCBI36
NG_008274.1:g.5056_5059del

Transcript Alleles

HGVS	Amino-acid Change
NM_001126121.2:c.-169_-166del MANE Select	NP_001119593.1:n.-169_-166del
ENST00000416858.7:c.-169_-166del MANE Select	ENSP00000397818.2:n.-169_-166del
NM_001126121.1:c.-169_-166del	NP_001119593.1:n.-169_-166del
NM_001126122.1:c.-79_-76del	NP_001119594.1:n.-79_-76del
NM_001126122.2:c.-79_-76del	NP_001119594.1:n.-79_-76del
NM_021734.4:c.-153_-150del	NP_068380.3:n.-153_-150del
NM_021734.5:c.-153_-150del	NP_068380.3:n.-153_-150del
ENST00000320362.7:c.-191_-188del	ENSP00000319574.3:n.-191_-188del
ENST00000375261.8:c.-169_-166del	ENSP00000364410.4:n.-169_-166del
ENST00000579228.1:n.56_59del
ENST00000580151.5:c.-283_-280del	ENSP00000462299.1:n.-283_-280del
ENST00000580273.1:c.-212_-209del	ENSP00000463039.1:n.-212_-209del
ENST00000580994.5:c.-153_-150del	ENSP00000463795.1:n.-153_-150del
ENST00000584438.1:c.-423_-420del	ENSP00000464457.1:n.-423_-420del
XM_005257559.2:c.-283_-280del	XP_005257616.1:n.-283_-280del
XM_005257559.4:c.-283_-280del	XP_005257616.1:n.-283_-280del
XM_005257561.2:c.-173_-170del	XP_005257618.1:n.-173_-170del
XM_005257561.4:c.-173_-170del	XP_005257618.1:n.-173_-170del
XM_011525098.1:c.-153_-150del	XP_011523400.1:n.-153_-150del
XM_017024927.2:c.-212_-209del	XP_016880416.1:n.-212_-209del
XM_017024928.2:c.-169_-166del	XP_016880417.1:n.-169_-166del