Canonical Allele Identifier: CA338254769

Gene: ATP13A2

Linked Data

• gnomAD v4: 1-16996460-A-G
• MyVariant Identifiers: chr1:g.17322955A>G (hg19) ; chr1:g.16996460A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16996460A>G , CM000663.2:g.16996460A>G	GRCh38
NC_000001.10:g.17322955A>G , CM000663.1:g.17322955A>G	GRCh37
NC_000001.9:g.17195542A>G	NCBI36
NG_009054.1:g.20469T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.1232T>C MANE Select	ENSP00000327214.8:p.Ile411Thr
ENST00000326735.12:c.1232T>C	ENSP00000327214.8:p.Ile411Thr
ENST00000341676.9:c.1217T>C	ENSP00000341115.5:p.Ile406Thr
ENST00000452699.5:c.1217T>C	ENSP00000413307.1:p.Ile406Thr
ENST00000463860.5:n.840T>C
ENST00000502860.1:n.335-160T>C
ENST00000506174.5:c.374T>C	ENSP00000424393.1:p.Ile125Thr
ENST00000509392.1:n.235T>C
ENST00000617114.4:c.335-160T>C	ENSP00000478781.1:n.335-160T>C
NM_001141973.2:c.1217T>C	NP_001135445.1:p.Ile406Thr
NM_001141974.2:c.1217T>C	NP_001135446.1:p.Ile406Thr
NM_022089.3:c.1232T>C	NP_071372.1:p.Ile411Thr
XM_005245809.1:c.1232T>C	XP_005245866.1:p.Ile411Thr
XM_005245810.1:c.1229T>C	XP_005245867.1:p.Ile410Thr
XM_005245811.1:c.1217T>C	XP_005245868.1:p.Ile406Thr
XM_005245812.1:c.1205T>C	XP_005245869.1:p.Ile402Thr
XM_005245813.1:c.1232T>C	XP_005245870.1:p.Ile411Thr
XM_005245815.1:c.1232T>C	XP_005245872.1:p.Ile411Thr
XM_006710512.1:c.1214T>C	XP_006710575.1:p.Ile405Thr
XM_006710513.1:c.1190T>C	XP_006710576.1:p.Ile397Thr
XM_011541128.1:c.1232T>C	XP_011539430.1:p.Ile411Thr
XM_011541129.1:c.1232T>C	XP_011539431.1:p.Ile411Thr
XM_017000844.1:c.1232T>C	XP_016856333.1:p.Ile411Thr
XM_017000845.1:c.1214T>C	XP_016856334.1:p.Ile405Thr
XM_017000846.1:c.1190T>C	XP_016856335.1:p.Ile397Thr
XM_017000847.1:c.1202T>C	XP_016856336.1:p.Ile401Thr
XM_017000848.1:c.1232T>C	XP_016856337.1:p.Ile411Thr
XM_017000849.1:c.1217T>C	XP_016856338.1:p.Ile406Thr
XM_017000850.1:c.1232T>C	XP_016856339.1:p.Ile411Thr
NM_022089.4:c.1232T>C MANE Select	NP_071372.1:p.Ile411Thr
NM_001141973.3:c.1217T>C	NP_001135445.1:p.Ile406Thr
NM_001141974.3:c.1217T>C	NP_001135446.1:p.Ile406Thr