Canonical Allele Identifier: CA416093630

Gene: ATP13A2

Linked Data

• MyVariant Identifiers: chr1:g.17313015G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16986520G>A , CM000663.2:g.16986520G>A	GRCh38
NC_000001.10:g.17313015G>A , CM000663.1:g.17313015G>A	GRCh37
NC_000001.9:g.17185602G>A	NCBI36
NG_009054.1:g.30409C>T
NG_029688.1:g.67C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326735.13:c.3348C>T MANE Select	ENSP00000327214.8:p.Phe1116=
ENST00000326735.12:c.3348C>T	ENSP00000327214.8:p.Phe1116=
ENST00000341676.9:c.3104-162C>T	ENSP00000341115.5:n.3104-162C>T
ENST00000452699.5:c.3333C>T	ENSP00000413307.1:p.Phe1111=
ENST00000466561.1:n.1394C>T
ENST00000502418.1:c.824-162C>T	ENSP00000423065.1:n.824-162C>T
NM_001141973.2:c.3333C>T	NP_001135445.1:p.Phe1111=
NM_001141974.2:c.3104-162C>T	NP_001135446.1:n.3104-162C>T
NM_022089.3:c.3348C>T	NP_071372.1:p.Phe1116=
XM_005245809.1:c.3236-162C>T	XP_005245866.1:n.3236-162C>T
XM_005245810.1:c.3233-162C>T	XP_005245867.1:n.3233-162C>T
XM_005245811.1:c.3221-162C>T	XP_005245868.1:n.3221-162C>T
XM_005245812.1:c.3209-162C>T	XP_005245869.1:n.3209-162C>T
XM_005245813.1:c.3176-162C>T	XP_005245870.1:n.3176-162C>T
XM_005245815.1:c.3119-162C>T	XP_005245872.1:n.3119-162C>T
XM_006710512.1:c.3218-162C>T	XP_006710575.1:n.3218-162C>T
XM_006710513.1:c.3194-162C>T	XP_006710576.1:n.3194-162C>T
XM_011541128.1:c.3221-162C>T	XP_011539430.1:n.3221-162C>T
XM_011541129.1:c.3029-162C>T	XP_011539431.1:n.3029-162C>T
XM_017000844.1:c.3333C>T	XP_016856333.1:p.Phe1111=
XM_017000845.1:c.3330C>T	XP_016856334.1:p.Phe1110=
XM_017000846.1:c.3306C>T	XP_016856335.1:p.Phe1102=
XM_017000847.1:c.3303C>T	XP_016856336.1:p.Phe1101=
XM_017000848.1:c.3231C>T	XP_016856337.1:p.Phe1077=
XM_017000849.1:c.3216C>T	XP_016856338.1:p.Phe1072=
XM_017000850.1:c.3141C>T	XP_016856339.1:p.Phe1047=
NM_022089.4:c.3348C>T MANE Select	NP_071372.1:p.Phe1116=
NM_001141973.3:c.3333C>T	NP_001135445.1:p.Phe1111=
NM_001141974.3:c.3104-162C>T	NP_001135446.1:n.3104-162C>T