Canonical Allele Identifier: CA5255947

Gene: SLC25A25

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128106391G>C , CM000671.2:g.128106391G>C	GRCh38
NC_000009.11:g.130868670G>C , CM000671.1:g.130868670G>C	GRCh37
NC_000009.10:g.129908491G>C	NCBI36
NG_032871.1:g.43192G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001330988.2:c.1083G>C MANE Select	NP_001317917.1:p.Gln361His
ENST00000373069.10:c.1083G>C MANE Select	ENSP00000362160.5:p.Gln361His
NM_001006641.3:c.1047G>C	NP_001006642.1:p.Gln349His
NM_001006641.4:c.1047G>C	NP_001006642.1:p.Gln349His
NM_001006642.3:c.1005G>C	NP_001006643.1:p.Gln335His
NM_001006642.4:c.1005G>C	NP_001006643.1:p.Gln335His
NM_001265614.2:c.1041G>C	NP_001252543.1:p.Gln347His
NM_001265614.3:c.1041G>C	NP_001252543.1:p.Gln347His
NM_001330988.1:c.1083G>C	NP_001317917.1:p.Gln361His
NM_001387057.1:c.981G>C	NP_001373986.1:p.Gln327His
NM_052901.4:c.945G>C	NP_443133.2:p.Gln315His
NM_052901.5:c.945G>C	NP_443133.2:p.Gln315His
NR_049766.2:n.1073G>C
NR_049766.3:n.1048G>C
ENST00000373064.9:c.945G>C	ENSP00000362155.5:p.Gln315His
ENST00000373066.9:c.1041G>C	ENSP00000362157.5:p.Gln347His
ENST00000373068.6:c.1047G>C	ENSP00000362159.2:p.Gln349His
ENST00000373069.9:c.1083G>C	ENSP00000362160.5:p.Gln361His
ENST00000432073.6:c.1005G>C	ENSP00000410053.2:p.Gln335His
ENST00000466983.1:c.157G>C
ENST00000682371.1:c.1161G>C	ENSP00000508277.1:p.Gln387His
ENST00000682638.1:n.1326G>C
ENST00000683206.1:c.672G>C	ENSP00000506909.1:p.Gln224His
XM_005251688.1:c.1083G>C	XP_005251745.1:p.Gln361His
XM_005251689.3:c.636G>C	XP_005251746.1:p.Gln212His
XM_006716948.1:c.981G>C	XP_006717011.1:p.Gln327His
XM_006716948.3:c.981G>C	XP_006717011.1:p.Gln327His
XM_006716949.2:c.672G>C	XP_006717012.1:p.Gln224His
XM_006716949.3:c.672G>C	XP_006717012.1:p.Gln224His
XR_002956752.1:n.1203G>C
XR_002956753.1:n.1167G>C
XR_002956754.1:n.1436G>C
XR_002956755.1:n.1400G>C
XR_002956756.1:n.1953G>C
XR_002956757.1:n.1001G>C
XR_002956758.1:n.1470G>C
XR_002956759.1:n.1432G>C