Canonical Allele Identifier: CA394382889

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2161625A>C (hg19) ; chr16:g.2111624A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2111624A>C , CM000678.2:g.2111624A>C	GRCh38
NC_000016.9:g.2161625A>C , CM000678.1:g.2161625A>C	GRCh37
NC_000016.8:g.2101626A>C	NCBI36
NG_008617.1:g.29275T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.3543T>G MANE Select	ENSP00000262304.4:p.Tyr1181Ter
ENST00000262304.8:c.3543T>G	ENSP00000262304.4:p.Tyr1181Ter
ENST00000415938.7:n.310+716T>G
ENST00000423118.5:c.3543T>G	ENSP00000399501.1:p.Tyr1181Ter
ENST00000468674.5:n.430+716T>G
ENST00000469241.2:n.493T>G
ENST00000483024.1:c.233+192T>G
ENST00000483731.5:n.790+716T>G
ENST00000488185.2:c.473-3266T>G
ENST00000565639.6:n.773+716T>G
ENST00000568591.5:c.2226+716T>G	ENSP00000457162.1:n.2226+716T>G
ENST00000569983.5:n.421+716T>G
NM_000296.3:c.3543T>G	NP_000287.3:p.Tyr1181Ter
NM_001009944.2:c.3543T>G	NP_001009944.2:p.Tyr1181Ter
XM_005255370.2:c.498T>G	XP_005255427.1:p.Tyr166Ter
XM_011522525.1:c.3621T>G	XP_011520827.1:p.Tyr1207Ter
XM_011522526.1:c.3621T>G	XP_011520828.1:p.Tyr1207Ter
XM_011522527.1:c.3621T>G	XP_011520829.1:p.Tyr1207Ter
XM_011522528.1:c.3597T>G	XP_011520830.1:p.Tyr1199Ter
XM_011522529.1:c.3597T>G	XP_011520831.1:p.Tyr1199Ter
XM_011522530.1:c.3567T>G	XP_011520832.1:p.Tyr1189Ter
XM_011522531.1:c.3549T>G	XP_011520833.1:p.Tyr1183Ter
XM_011522532.1:c.3495T>G	XP_011520834.1:p.Tyr1165Ter
XM_011522533.1:c.3414T>G	XP_011520835.1:p.Tyr1138Ter
XM_011522534.1:c.3357T>G	XP_011520836.1:p.Tyr1119Ter
XM_011522535.1:c.1443T>G	XP_011520837.1:p.Tyr481Ter
XM_011522536.1:c.3621T>G	XP_011520838.1:p.Tyr1207Ter
XM_011522537.1:c.621T>G	XP_011520839.1:p.Tyr207Ter
XR_932867.1:n.3636T>G
XR_932868.1:n.3636T>G
XR_932869.1:n.3636T>G
XR_932870.1:n.3636T>G
XM_005255370.3:c.498T>G	XP_005255427.1:p.Tyr166Ter
XM_011522528.3:c.3597T>G	XP_011520830.1:p.Tyr1199Ter
XM_011522529.2:c.3597T>G	XP_011520831.1:p.Tyr1199Ter
XM_011522537.2:c.621T>G	XP_011520839.1:p.Tyr207Ter
XM_024450298.1:c.3663T>G	XP_024306066.1:p.Tyr1221Ter
XM_024450299.1:c.3591T>G	XP_024306067.1:p.Tyr1197Ter
XM_024450300.1:c.3453T>G	XP_024306068.1:p.Tyr1151Ter
XM_024450301.1:c.1539T>G	XP_024306069.1:p.Tyr513Ter
NM_000296.4:c.3543T>G	NP_000287.4:p.Tyr1181Ter
NM_001009944.3:c.3543T>G MANE Select	NP_001009944.3:p.Tyr1181Ter