Canonical Allele Identifier: CA413037411

Gene: SLC9A7

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.46662612A>C , CM000685.2:g.46662612A>C	GRCh38
NC_000023.10:g.46522047A>C , CM000685.1:g.46522047A>C	GRCh37
NC_000023.9:g.46406991A>C	NCBI36
NG_012622.2:g.101426T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001257291.2:c.825T>G MANE Select	NP_001244220.1:p.His275Gln
ENST00000616978.5:c.825T>G MANE Select	ENSP00000480916.1:p.His275Gln
NM_001257291.1:c.825T>G	NP_001244220.1:p.His275Gln
NM_032591.2:c.825T>G	NP_115980.1:p.His275Gln
NM_032591.3:c.825T>G	NP_115980.1:p.His275Gln
ENST00000328306.4:c.825T>G	ENSP00000330320.4:p.His275Gln
ENST00000489574.2:n.80+6995T>G
ENST00000616978.4:c.825T>G	ENSP00000480916.1:p.His275Gln
XM_005272681.3:c.825T>G	XP_005272738.1:p.His275Gln
XM_005272681.4:c.825T>G	XP_005272738.1:p.His275Gln
XM_005272682.3:c.825T>G	XP_005272739.1:p.His275Gln
XM_005272682.4:c.825T>G	XP_005272739.1:p.His275Gln
XM_006724564.2:c.825T>G	XP_006724627.1:p.His275Gln
XM_006724564.4:c.825T>G	XP_006724627.1:p.His275Gln
XM_011543990.1:c.825T>G	XP_011542292.1:p.His275Gln
XM_011543990.2:c.825T>G	XP_011542292.1:p.His275Gln
XM_011543991.1:c.825T>G	XP_011542293.1:p.His275Gln
XM_011543992.1:c.825T>G	XP_011542294.1:p.His275Gln
XM_017029905.1:c.825T>G	XP_016885394.1:p.His275Gln
XM_017029906.2:c.825T>G	XP_016885395.1:p.His275Gln
XR_002958808.1:n.958T>G