Canonical Allele Identifier: CA394382941

Gene: PKD1

Linked Data

• gnomAD v4: 16-2111648-G-T
• MyVariant Identifiers: chr16:g.2161649G>T (hg19) ; chr16:g.2111648G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2111648G>T , CM000678.2:g.2111648G>T	GRCh38
NC_000016.9:g.2161649G>T , CM000678.1:g.2161649G>T	GRCh37
NC_000016.8:g.2101650G>T	NCBI36
NG_008617.1:g.29251C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.3519C>A MANE Select	ENSP00000262304.4:p.Ser1173Arg
ENST00000262304.8:c.3519C>A	ENSP00000262304.4:p.Ser1173Arg
ENST00000415938.7:n.310+692C>A
ENST00000423118.5:c.3519C>A	ENSP00000399501.1:p.Ser1173Arg
ENST00000468674.5:n.430+692C>A
ENST00000469241.2:n.469C>A
ENST00000483024.1:c.233+168C>A
ENST00000483731.5:n.790+692C>A
ENST00000488185.2:c.473-3290C>A
ENST00000565639.6:n.773+692C>A
ENST00000568591.5:c.2226+692C>A	ENSP00000457162.1:n.2226+692C>A
ENST00000569983.5:n.421+692C>A
NM_000296.3:c.3519C>A	NP_000287.3:p.Ser1173Arg
NM_001009944.2:c.3519C>A	NP_001009944.2:p.Ser1173Arg
XM_005255370.2:c.474C>A	XP_005255427.1:p.Ser158Arg
XM_011522525.1:c.3597C>A	XP_011520827.1:p.Ser1199Arg
XM_011522526.1:c.3597C>A	XP_011520828.1:p.Ser1199Arg
XM_011522527.1:c.3597C>A	XP_011520829.1:p.Ser1199Arg
XM_011522528.1:c.3573C>A	XP_011520830.1:p.Ser1191Arg
XM_011522529.1:c.3573C>A	XP_011520831.1:p.Ser1191Arg
XM_011522530.1:c.3543C>A	XP_011520832.1:p.Ser1181Arg
XM_011522531.1:c.3525C>A	XP_011520833.1:p.Ser1175Arg
XM_011522532.1:c.3471C>A	XP_011520834.1:p.Ser1157Arg
XM_011522533.1:c.3390C>A	XP_011520835.1:p.Ser1130Arg
XM_011522534.1:c.3333C>A	XP_011520836.1:p.Ser1111Arg
XM_011522535.1:c.1419C>A	XP_011520837.1:p.Ser473Arg
XM_011522536.1:c.3597C>A	XP_011520838.1:p.Ser1199Arg
XM_011522537.1:c.597C>A	XP_011520839.1:p.Ser199Arg
XR_932867.1:n.3612C>A
XR_932868.1:n.3612C>A
XR_932869.1:n.3612C>A
XR_932870.1:n.3612C>A
XM_005255370.3:c.474C>A	XP_005255427.1:p.Ser158Arg
XM_011522528.3:c.3573C>A	XP_011520830.1:p.Ser1191Arg
XM_011522529.2:c.3573C>A	XP_011520831.1:p.Ser1191Arg
XM_011522537.2:c.597C>A	XP_011520839.1:p.Ser199Arg
XM_024450298.1:c.3639C>A	XP_024306066.1:p.Ser1213Arg
XM_024450299.1:c.3567C>A	XP_024306067.1:p.Ser1189Arg
XM_024450300.1:c.3429C>A	XP_024306068.1:p.Ser1143Arg
XM_024450301.1:c.1515C>A	XP_024306069.1:p.Ser505Arg
NM_000296.4:c.3519C>A	NP_000287.4:p.Ser1173Arg
NM_001009944.3:c.3519C>A MANE Select	NP_001009944.3:p.Ser1173Arg