Canonical Allele Identifier: CA394382957

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2161657T>A (hg19) ; chr16:g.2111656T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2111656T>A , CM000678.2:g.2111656T>A	GRCh38
NC_000016.9:g.2161657T>A , CM000678.1:g.2161657T>A	GRCh37
NC_000016.8:g.2101658T>A	NCBI36
NG_008617.1:g.29243A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.3511A>T MANE Select	ENSP00000262304.4:p.Thr1171Ser
ENST00000262304.8:c.3511A>T	ENSP00000262304.4:p.Thr1171Ser
ENST00000415938.7:n.310+684A>T
ENST00000423118.5:c.3511A>T	ENSP00000399501.1:p.Thr1171Ser
ENST00000468674.5:n.430+684A>T
ENST00000469241.2:n.461A>T
ENST00000483024.1:c.233+160A>T
ENST00000483731.5:n.790+684A>T
ENST00000488185.2:c.473-3298A>T
ENST00000565639.6:n.773+684A>T
ENST00000568591.5:c.2226+684A>T	ENSP00000457162.1:n.2226+684A>T
ENST00000569983.5:n.421+684A>T
NM_000296.3:c.3511A>T	NP_000287.3:p.Thr1171Ser
NM_001009944.2:c.3511A>T	NP_001009944.2:p.Thr1171Ser
XM_005255370.2:c.466A>T	XP_005255427.1:p.Thr156Ser
XM_011522525.1:c.3589A>T	XP_011520827.1:p.Thr1197Ser
XM_011522526.1:c.3589A>T	XP_011520828.1:p.Thr1197Ser
XM_011522527.1:c.3589A>T	XP_011520829.1:p.Thr1197Ser
XM_011522528.1:c.3565A>T	XP_011520830.1:p.Thr1189Ser
XM_011522529.1:c.3565A>T	XP_011520831.1:p.Thr1189Ser
XM_011522530.1:c.3535A>T	XP_011520832.1:p.Thr1179Ser
XM_011522531.1:c.3517A>T	XP_011520833.1:p.Thr1173Ser
XM_011522532.1:c.3463A>T	XP_011520834.1:p.Thr1155Ser
XM_011522533.1:c.3382A>T	XP_011520835.1:p.Thr1128Ser
XM_011522534.1:c.3325A>T	XP_011520836.1:p.Thr1109Ser
XM_011522535.1:c.1411A>T	XP_011520837.1:p.Thr471Ser
XM_011522536.1:c.3589A>T	XP_011520838.1:p.Thr1197Ser
XM_011522537.1:c.589A>T	XP_011520839.1:p.Thr197Ser
XR_932867.1:n.3604A>T
XR_932868.1:n.3604A>T
XR_932869.1:n.3604A>T
XR_932870.1:n.3604A>T
XM_005255370.3:c.466A>T	XP_005255427.1:p.Thr156Ser
XM_011522528.3:c.3565A>T	XP_011520830.1:p.Thr1189Ser
XM_011522529.2:c.3565A>T	XP_011520831.1:p.Thr1189Ser
XM_011522537.2:c.589A>T	XP_011520839.1:p.Thr197Ser
XM_024450298.1:c.3631A>T	XP_024306066.1:p.Thr1211Ser
XM_024450299.1:c.3559A>T	XP_024306067.1:p.Thr1187Ser
XM_024450300.1:c.3421A>T	XP_024306068.1:p.Thr1141Ser
XM_024450301.1:c.1507A>T	XP_024306069.1:p.Thr503Ser
NM_000296.4:c.3511A>T	NP_000287.4:p.Thr1171Ser
NM_001009944.3:c.3511A>T MANE Select	NP_001009944.3:p.Thr1171Ser