Canonical Allele Identifier: CA1826277101

Gene: SLC52A2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144360366G= , CM000670.2:g.144360366G=	GRCh38
NC_000008.10:g.145584026G= , CM000670.1:g.145584026G=	GRCh37
NC_000008.9:g.145554834G=	NCBI36
NG_032872.1:g.6810G=
NG_032872.2:g.6810G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329994.7:c.874G=	ENSP00000333638.2:p.Gly292=
ENST00000526338.7:c.382G=	ENSP00000433583.3:p.Gly128=
ENST00000526752.3:c.131-437G=	ENSP00000433796.1:n.131-437G=
ENST00000526779.3:c.*186G=	ENSP00000436917.1:n.*186G=
ENST00000526891.2:c.610G=	ENSP00000502670.1:p.Gly204=
ENST00000527078.6:c.874G=	ENSP00000434728.1:p.Gly292=
ENST00000532815.2:c.874G=	ENSP00000501933.1:p.Gly292=
ENST00000533662.2:c.874G=	ENSP00000502274.1:p.Gly292=
ENST00000534725.6:c.874G=	ENSP00000431965.2:p.Gly292=
ENST00000643944.2:c.874G= MANE Select	ENSP00000496184.2:p.Gly292=
ENST00000674779.1:c.*186G=	ENSP00000501929.1:n.*186G=
ENST00000674821.1:c.*678G=	ENSP00000502219.1:n.*678G=
ENST00000674870.1:c.874G=	ENSP00000502406.1:p.Gly292=
ENST00000674929.1:c.382G=	ENSP00000501554.1:p.Gly128=
ENST00000675121.1:c.874G=	ENSP00000501993.1:p.Gly292=
ENST00000675280.1:c.874G=	ENSP00000502796.1:p.Gly292=
ENST00000675292.1:c.874G=	ENSP00000502652.1:p.Gly292=
ENST00000675597.1:c.382G=	ENSP00000501973.1:p.Gly128=
ENST00000675787.1:c.874G=	ENSP00000502189.1:p.Gly292=
ENST00000675888.1:c.874G=	ENSP00000502294.1:p.Gly292=
ENST00000675998.1:n.426G=
ENST00000676094.1:c.325G=	ENSP00000502066.1:p.Gly109=
ENST00000676358.1:c.*186G=	ENSP00000501821.1:n.*186G=
ENST00000329994.6:c.874G=	ENSP00000333638.2:p.Gly292=
ENST00000402965.5:c.874G=	ENSP00000385961.1:p.Gly292=
ENST00000526338.5:c.382G=	ENSP00000433583.1:p.Gly128=
ENST00000526752.1:c.131-437G=	ENSP00000433796.1:n.131-437G=
ENST00000526779.1:c.*186G=	ENSP00000436917.1:n.*186G=
ENST00000527078.5:c.874G=	ENSP00000434728.1:p.Gly292=
ENST00000530047.5:c.874G=	ENSP00000435820.1:p.Gly292=
ENST00000532887.5:c.874G=	ENSP00000436768.1:p.Gly292=
NM_001253815.1:c.874G=	NP_001240744.1:p.Gly292=
NM_001253816.1:c.874G=	NP_001240745.1:p.Gly292=
NM_024531.4:c.874G=	NP_078807.1:p.Gly292=
NR_045600.1:n.1366G=
XM_006716658.1:c.874G=	XP_006716721.1:p.Gly292=
XM_006716659.1:c.874G=	XP_006716722.1:p.Gly292=
XM_006716660.1:c.874G=	XP_006716723.1:p.Gly292=
XM_011517300.1:c.610G=	XP_011515602.1:p.Gly204=
NM_001363118.1:c.874G=	NP_001350047.1:p.Gly292=
NM_001363120.1:c.874G=	NP_001350049.1:p.Gly292=
NM_001363121.1:c.874G=	NP_001350050.1:p.Gly292=
NM_001363122.1:c.382G=	NP_001350051.1:p.Gly128=
XM_011517300.2:c.610G=	XP_011515602.1:p.Gly204=
XM_017013821.1:c.382G=	XP_016869310.1:p.Gly128=
XM_017013822.1:c.382G=	XP_016869311.1:p.Gly128=
NM_001253815.2:c.874G=	NP_001240744.1:p.Gly292=
NM_001253816.2:c.874G=	NP_001240745.1:p.Gly292=
NM_001363118.2:c.874G= MANE Select	NP_001350047.1:p.Gly292=
NM_001363120.2:c.874G=	NP_001350049.1:p.Gly292=
NM_001363121.2:c.874G=	NP_001350050.1:p.Gly292=
NM_001363122.2:c.382G=	NP_001350051.1:p.Gly128=
NM_024531.5:c.874G=	NP_078807.1:p.Gly292=
NR_045600.2:n.1334G=