Canonical Allele Identifier: CA2202017961

Gene: PKD1 PKD1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2091702_2091703delinsCG , CM000678.2:g.2091702_2091703delinsCG	GRCh38
NC_000016.9:g.2141703_2141704delinsCG , CM000678.1:g.2141703_2141704delinsCG	GRCh37
NC_000016.8:g.2081704_2081705delinsCG	NCBI36
NG_008617.1:g.51518_51519delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000262304.9:c.11537+78_11537+79delinsCG (PKD1) MANE Select	ENSP00000262304.4:n.11537+78_11537+79deli...
ENST00000262304.8:c.11537+78_11537+79delinsCG (PKD1)	ENSP00000262304.4:n.11537+78_11537+79deli...
ENST00000423118.5:c.11534+78_11534+79delinsCG (PKD1)	ENSP00000399501.1:n.11534+78_11534+79deli...
ENST00000485120.1:n.526+78_526+79delinsCG (PKD1)
ENST00000487932.5:c.6099+78_6099+79delinsCG (PKD1)	ENSP00000457132.1:n.6099+78_6099+79delins...
ENST00000561668.5:c.198+78_198+79delinsCG (PKD1)
ENST00000564313.1:n.233+78_233+79delinsCG (PKD1)
NM_000296.3:c.11534+78_11534+79delinsCG (PKD1)	NP_000287.3:n.11534+78_11534+79delinsCG
NM_001009944.2:c.11537+78_11537+79delinsCG (PKD1)	NP_001009944.2:n.11537+78_11537+79delinsC...
XM_005255370.2:c.8492+78_8492+79delinsCG (PKD1)	XP_005255427.1:n.8492+78_8492+79delinsCG
XM_011522525.1:c.11615+78_11615+79delinsCG (PKD1)	XP_011520827.1:n.11615+78_11615+79delinsC...
XM_011522526.1:c.11612+78_11612+79delinsCG (PKD1)	XP_011520828.1:n.11612+78_11612+79delinsC...
XM_011522527.1:c.11597+78_11597+79delinsCG (PKD1)	XP_011520829.1:n.11597+78_11597+79delinsC...
XM_011522528.1:c.11591+78_11591+79delinsCG (PKD1)	XP_011520830.1:n.11591+78_11591+79delinsC...
XM_011522529.1:c.11588+78_11588+79delinsCG (PKD1)	XP_011520831.1:n.11588+78_11588+79delinsC...
XM_011522530.1:c.11561+78_11561+79delinsCG (PKD1)	XP_011520832.1:n.11561+78_11561+79delinsC...
XM_011522531.1:c.11543+78_11543+79delinsCG (PKD1)	XP_011520833.1:n.11543+78_11543+79delinsC...
XM_011522532.1:c.11489+78_11489+79delinsCG (PKD1)	XP_011520834.1:n.11489+78_11489+79delinsC...
XM_011522533.1:c.11408+78_11408+79delinsCG (PKD1)	XP_011520835.1:n.11408+78_11408+79delinsC...
XM_011522534.1:c.11351+78_11351+79delinsCG (PKD1)	XP_011520836.1:n.11351+78_11351+79delinsC...
XM_011522535.1:c.9437+78_9437+79delinsCG (PKD1)	XP_011520837.1:n.9437+78_9437+79delinsCG
XM_011522537.1:c.8615+78_8615+79delinsCG (PKD1)	XP_011520839.1:n.8615+78_8615+79delinsCG
XR_932867.1:n.11630+78_11630+79delinsCG (PKD1)
XR_932868.1:n.11377+78_11377+79delinsCG (PKD1)
XR_932869.1:n.11377+78_11377+79delinsCG (PKD1)
XR_933000.1:n.89+88_89+89delinsCG (PKD1-AS1)
XR_933001.1:n.179+88_179+89delinsCG (PKD1-AS1)
XR_933002.1:n.88+94_88+95delinsCG (PKD1-AS1)
XR_933003.1:n.88+94_88+95delinsCG (PKD1-AS1)
NR_135175.1:n.179+88_179+89delinsCG (PKD1-AS1)
XM_005255370.3:c.8492+78_8492+79delinsCG (PKD1)	XP_005255427.1:n.8492+78_8492+79delinsCG
XM_011522528.3:c.11591+78_11591+79delinsCG (PKD1)	XP_011520830.1:n.11591+78_11591+79delinsC...
XM_011522529.2:c.11588+78_11588+79delinsCG (PKD1)	XP_011520831.1:n.11588+78_11588+79delinsC...
XM_011522537.2:c.8615+78_8615+79delinsCG (PKD1)	XP_011520839.1:n.8615+78_8615+79delinsCG
XM_024450298.1:c.11657+78_11657+79delinsCG (PKD1)	XP_024306066.1:n.11657+78_11657+79delinsC...
XM_024450299.1:c.11585+78_11585+79delinsCG (PKD1)	XP_024306067.1:n.11585+78_11585+79delinsC...
XM_024450300.1:c.11447+78_11447+79delinsCG (PKD1)	XP_024306068.1:n.11447+78_11447+79delinsC...
XM_024450301.1:c.9533+78_9533+79delinsCG (PKD1)	XP_024306069.1:n.9533+78_9533+79delinsCG
NM_000296.4:c.11534+78_11534+79delinsCG (PKD1)	NP_000287.4:n.11534+78_11534+79delinsCG
NM_001009944.3:c.11537+78_11537+79delinsCG (PKD1) MANE Select	NP_001009944.3:n.11537+78_11537+79delinsC...