Canonical Allele Identifier: CA352204323

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39394388_39394389del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394389_39394390del , CM000665.2:g.39394389_39394390del	GRCh38
NC_000003.11:g.39435880_39435881del , CM000665.1:g.39435880_39435881del	GRCh37
NC_000003.10:g.39410884_39410885del	NCBI36
NG_016931.1:g.16066_16067del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.578-21_578-20del	ENSP00000495376.1:n.578-21_578-20del
ENST00000643672.1:c.575-21_575-20del	ENSP00000494532.1:n.575-21_575-20del
ENST00000645280.1:c.572-21_572-20del	ENSP00000496690.1:n.572-21_572-20del
ENST00000645630.1:c.446-21_446-20del	ENSP00000493714.1:n.446-21_446-20del
ENST00000648579.1:c.722-61_722-60del	ENSP00000497638.1:n.722-61_722-60del
ENST00000650617.1:c.626-21_626-20del MANE Select	ENSP00000497532.1:n.626-21_626-20del
ENST00000273158.8:c.626-21_626-20del	ENSP00000273158.3:n.626-21_626-20del
NM_017875.2:c.626-21_626-20del	NP_060345.2:n.626-21_626-20del
XM_006713214.1:c.614-21_614-20del	XP_006713277.1:n.614-21_614-20del
XM_011533869.1:c.608-21_608-20del	XP_011532171.1:n.608-21_608-20del
XM_011533870.1:c.575-21_575-20del	XP_011532172.1:n.575-21_575-20del
XM_011533871.1:c.446-21_446-20del	XP_011532173.1:n.446-21_446-20del
NM_001354798.1:c.626-2009_626-2008del	NP_001341727.1:n.626-2009_626-2008del
NM_017875.4:c.626-21_626-20del MANE Select	NP_060345.2:n.626-21_626-20del
XM_006713214.2:c.614-21_614-20del	XP_006713277.1:n.614-21_614-20del
XM_011533869.2:c.608-21_608-20del	XP_011532171.1:n.608-21_608-20del
XM_024453611.1:c.572-21_572-20del	XP_024309379.1:n.572-21_572-20del
NM_001354798.2:c.626-2009_626-2008del	NP_001341727.1:n.626-2009_626-2008del