Canonical Allele Identifier: CA1156031676

Gene: ATP13A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16996466_16996469delinsCTCA , CM000663.2:g.16996466_16996469delinsCTCA	GRCh38
NC_000001.10:g.17322961_17322964delinsCTCA , CM000663.1:g.17322961_17322964delinsCTCA	GRCh37
NC_000001.9:g.17195548_17195551delinsCTCA	NCBI36
NG_009054.1:g.20460_20463delinsTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326735.13:c.1223_1226delinsTGAG MANE Select	ENSP00000327214.8:p.Val408=
ENST00000326735.12:c.1223_1226delinsTGAG	ENSP00000327214.8:p.Val408=
ENST00000341676.9:c.1208_1211delinsTGAG	ENSP00000341115.5:p.Val403=
ENST00000452699.5:c.1208_1211delinsTGAG	ENSP00000413307.1:p.Val403=
ENST00000463860.5:n.831_834delinsTGAG
ENST00000502860.1:n.335-169_335-166delinsTGAG
ENST00000506174.5:c.365_368delinsTGAG	ENSP00000424393.1:p.Val122=
ENST00000509392.1:n.226_229delinsTGAG
ENST00000617114.4:c.335-169_335-166delinsTGAG	ENSP00000478781.1:n.335-169_335-166delinsTGAG
NM_001141973.2:c.1208_1211delinsTGAG	NP_001135445.1:p.Val403=
NM_001141974.2:c.1208_1211delinsTGAG	NP_001135446.1:p.Val403=
NM_022089.3:c.1223_1226delinsTGAG	NP_071372.1:p.Val408=
XM_005245809.1:c.1223_1226delinsTGAG	XP_005245866.1:p.Val408=
XM_005245810.1:c.1220_1223delinsTGAG	XP_005245867.1:p.Val407=
XM_005245811.1:c.1208_1211delinsTGAG	XP_005245868.1:p.Val403=
XM_005245812.1:c.1196_1199delinsTGAG	XP_005245869.1:p.Val399=
XM_005245813.1:c.1223_1226delinsTGAG	XP_005245870.1:p.Val408=
XM_005245815.1:c.1223_1226delinsTGAG	XP_005245872.1:p.Val408=
XM_006710512.1:c.1205_1208delinsTGAG	XP_006710575.1:p.Val402=
XM_006710513.1:c.1181_1184delinsTGAG	XP_006710576.1:p.Val394=
XM_011541128.1:c.1223_1226delinsTGAG	XP_011539430.1:p.Val408=
XM_011541129.1:c.1223_1226delinsTGAG	XP_011539431.1:p.Val408=
XM_017000844.1:c.1223_1226delinsTGAG	XP_016856333.1:p.Val408=
XM_017000845.1:c.1205_1208delinsTGAG	XP_016856334.1:p.Val402=
XM_017000846.1:c.1181_1184delinsTGAG	XP_016856335.1:p.Val394=
XM_017000847.1:c.1193_1196delinsTGAG	XP_016856336.1:p.Val398=
XM_017000848.1:c.1223_1226delinsTGAG	XP_016856337.1:p.Val408=
XM_017000849.1:c.1208_1211delinsTGAG	XP_016856338.1:p.Val403=
XM_017000850.1:c.1223_1226delinsTGAG	XP_016856339.1:p.Val408=
NM_022089.4:c.1223_1226delinsTGAG MANE Select	NP_071372.1:p.Val408=
NM_001141973.3:c.1208_1211delinsTGAG	NP_001135445.1:p.Val403=
NM_001141974.3:c.1208_1211delinsTGAG	NP_001135446.1:p.Val403=