Canonical Allele Identifier: CA1358939221

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394252_39394253delinsAC , CM000665.2:g.39394252_39394253delinsAC	GRCh38
NC_000003.11:g.39435743_39435744delinsAC , CM000665.1:g.39435743_39435744delinsAC	GRCh37
NC_000003.10:g.39410747_39410748delinsAC	NCBI36
NG_016931.1:g.15929_15930delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.578-158_578-157delinsAC	ENSP00000495376.1:n.578-158_578-157delinsAC
ENST00000643672.1:c.575-158_575-157delinsAC	ENSP00000494532.1:n.575-158_575-157delinsAC
ENST00000645280.1:c.572-158_572-157delinsAC	ENSP00000496690.1:n.572-158_572-157delinsAC
ENST00000645630.1:c.446-158_446-157delinsAC	ENSP00000493714.1:n.446-158_446-157delinsAC
ENST00000648579.1:c.722-198_722-197delinsAC	ENSP00000497638.1:n.722-198_722-197delinsAC
ENST00000650617.1:c.626-158_626-157delinsAC MANE Select	ENSP00000497532.1:n.626-158_626-157delinsAC
ENST00000273158.8:c.626-158_626-157delinsAC	ENSP00000273158.3:n.626-158_626-157delinsAC
NM_017875.2:c.626-158_626-157delinsAC	NP_060345.2:n.626-158_626-157delinsAC
XM_006713214.1:c.614-158_614-157delinsAC	XP_006713277.1:n.614-158_614-157delinsAC
XM_011533869.1:c.608-158_608-157delinsAC	XP_011532171.1:n.608-158_608-157delinsAC
XM_011533870.1:c.575-158_575-157delinsAC	XP_011532172.1:n.575-158_575-157delinsAC
XM_011533871.1:c.446-158_446-157delinsAC	XP_011532173.1:n.446-158_446-157delinsAC
NM_001354798.1:c.626-2146_626-2145delinsAC	NP_001341727.1:n.626-2146_626-2145delinsAC
NM_017875.4:c.626-158_626-157delinsAC MANE Select	NP_060345.2:n.626-158_626-157delinsAC
XM_006713214.2:c.614-158_614-157delinsAC	XP_006713277.1:n.614-158_614-157delinsAC
XM_011533869.2:c.608-158_608-157delinsAC	XP_011532171.1:n.608-158_608-157delinsAC
XM_024453611.1:c.572-158_572-157delinsAC	XP_024309379.1:n.572-158_572-157delinsAC
NM_001354798.2:c.626-2146_626-2145delinsAC	NP_001341727.1:n.626-2146_626-2145delinsAC