Canonical Allele Identifier: CA1358939216

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394235_39394236delinsAC , CM000665.2:g.39394235_39394236delinsAC	GRCh38
NC_000003.11:g.39435726_39435727delinsAC , CM000665.1:g.39435726_39435727delinsAC	GRCh37
NC_000003.10:g.39410730_39410731delinsAC	NCBI36
NG_016931.1:g.15912_15913delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.578-175_578-174delinsAC	ENSP00000495376.1:n.578-175_578-174delinsAC
ENST00000643672.1:c.575-175_575-174delinsAC	ENSP00000494532.1:n.575-175_575-174delinsAC
ENST00000645280.1:c.572-175_572-174delinsAC	ENSP00000496690.1:n.572-175_572-174delinsAC
ENST00000645630.1:c.446-175_446-174delinsAC	ENSP00000493714.1:n.446-175_446-174delinsAC
ENST00000648579.1:c.722-215_722-214delinsAC	ENSP00000497638.1:n.722-215_722-214delinsAC
ENST00000650617.1:c.626-175_626-174delinsAC MANE Select	ENSP00000497532.1:n.626-175_626-174delinsAC
ENST00000273158.8:c.626-175_626-174delinsAC	ENSP00000273158.3:n.626-175_626-174delinsAC
NM_017875.2:c.626-175_626-174delinsAC	NP_060345.2:n.626-175_626-174delinsAC
XM_006713214.1:c.614-175_614-174delinsAC	XP_006713277.1:n.614-175_614-174delinsAC
XM_011533869.1:c.608-175_608-174delinsAC	XP_011532171.1:n.608-175_608-174delinsAC
XM_011533870.1:c.575-175_575-174delinsAC	XP_011532172.1:n.575-175_575-174delinsAC
XM_011533871.1:c.446-175_446-174delinsAC	XP_011532173.1:n.446-175_446-174delinsAC
NM_001354798.1:c.626-2163_626-2162delinsAC	NP_001341727.1:n.626-2163_626-2162delinsAC
NM_017875.4:c.626-175_626-174delinsAC MANE Select	NP_060345.2:n.626-175_626-174delinsAC
XM_006713214.2:c.614-175_614-174delinsAC	XP_006713277.1:n.614-175_614-174delinsAC
XM_011533869.2:c.608-175_608-174delinsAC	XP_011532171.1:n.608-175_608-174delinsAC
XM_024453611.1:c.572-175_572-174delinsAC	XP_024309379.1:n.572-175_572-174delinsAC
NM_001354798.2:c.626-2163_626-2162delinsAC	NP_001341727.1:n.626-2163_626-2162delinsAC