Canonical Allele Identifier: CA394370013

Gene: PKD1

Linked Data

• gnomAD v4: 16-2106523-C-T
• MyVariant Identifiers: chr16:g.2156524C>T (hg19) ; chr16:g.2106523C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2106523C>T , CM000678.2:g.2106523C>T	GRCh38
NC_000016.9:g.2156524C>T , CM000678.1:g.2156524C>T	GRCh37
NC_000016.8:g.2096525C>T	NCBI36
NG_008617.1:g.34376G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.7364G>A MANE Select	ENSP00000262304.4:p.Gly2455Asp
ENST00000262304.8:c.7364G>A	ENSP00000262304.4:p.Gly2455Asp
ENST00000415938.7:n.609G>A
ENST00000423118.5:c.7364G>A	ENSP00000399501.1:p.Gly2455Asp
ENST00000483558.5:n.423G>A
ENST00000483731.5:n.1089G>A
ENST00000486339.6:n.1110G>A
ENST00000487932.5:c.2051G>A	ENSP00000457132.1:p.Gly684Asp
ENST00000496574.6:n.1367G>A
ENST00000565639.6:n.1072G>A
ENST00000568591.5:c.2525G>A	ENSP00000457162.1:n.2525G>A
ENST00000569983.5:n.720G>A
NM_000296.3:c.7364G>A	NP_000287.3:p.Gly2455Asp
NM_001009944.2:c.7364G>A	NP_001009944.2:p.Gly2455Asp
XM_005255370.2:c.4319G>A	XP_005255427.1:p.Gly1440Asp
XM_011522525.1:c.7442G>A	XP_011520827.1:p.Gly2481Asp
XM_011522526.1:c.7442G>A	XP_011520828.1:p.Gly2481Asp
XM_011522527.1:c.7442G>A	XP_011520829.1:p.Gly2481Asp
XM_011522528.1:c.7418G>A	XP_011520830.1:p.Gly2473Asp
XM_011522529.1:c.7418G>A	XP_011520831.1:p.Gly2473Asp
XM_011522530.1:c.7388G>A	XP_011520832.1:p.Gly2463Asp
XM_011522531.1:c.7370G>A	XP_011520833.1:p.Gly2457Asp
XM_011522532.1:c.7316G>A	XP_011520834.1:p.Gly2439Asp
XM_011522533.1:c.7235G>A	XP_011520835.1:p.Gly2412Asp
XM_011522534.1:c.7178G>A	XP_011520836.1:p.Gly2393Asp
XM_011522535.1:c.5264G>A	XP_011520837.1:p.Gly1755Asp
XM_011522536.1:c.7442G>A	XP_011520838.1:p.Gly2481Asp
XM_011522537.1:c.4442G>A	XP_011520839.1:p.Gly1481Asp
XR_932867.1:n.7457G>A
XR_932868.1:n.7457G>A
XR_932869.1:n.7457G>A
XR_932870.1:n.7457G>A
XM_005255370.3:c.4319G>A	XP_005255427.1:p.Gly1440Asp
XM_011522528.3:c.7418G>A	XP_011520830.1:p.Gly2473Asp
XM_011522529.2:c.7418G>A	XP_011520831.1:p.Gly2473Asp
XM_011522537.2:c.4442G>A	XP_011520839.1:p.Gly1481Asp
XM_024450298.1:c.7484G>A	XP_024306066.1:p.Gly2495Asp
XM_024450299.1:c.7412G>A	XP_024306067.1:p.Gly2471Asp
XM_024450300.1:c.7274G>A	XP_024306068.1:p.Gly2425Asp
XM_024450301.1:c.5360G>A	XP_024306069.1:p.Gly1787Asp
NM_000296.4:c.7364G>A	NP_000287.4:p.Gly2455Asp
NM_001009944.3:c.7364G>A MANE Select	NP_001009944.3:p.Gly2455Asp