Canonical Allele Identifier: CA394383058

Gene: PKD1

Linked Data

• MyVariant Identifiers: chr16:g.2161708G>C (hg19) ; chr16:g.2111707G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2111707G>C , CM000678.2:g.2111707G>C	GRCh38
NC_000016.9:g.2161708G>C , CM000678.1:g.2161708G>C	GRCh37
NC_000016.8:g.2101709G>C	NCBI36
NG_008617.1:g.29192C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.3460C>G MANE Select	ENSP00000262304.4:p.Pro1154Ala
ENST00000262304.8:c.3460C>G	ENSP00000262304.4:p.Pro1154Ala
ENST00000415938.7:n.310+633C>G
ENST00000423118.5:c.3460C>G	ENSP00000399501.1:p.Pro1154Ala
ENST00000468674.5:n.430+633C>G
ENST00000469241.2:n.410C>G
ENST00000483024.1:c.233+109C>G
ENST00000483731.5:n.790+633C>G
ENST00000488185.2:c.473-3349C>G
ENST00000565639.6:n.773+633C>G
ENST00000568591.5:c.2226+633C>G	ENSP00000457162.1:n.2226+633C>G
ENST00000569983.5:n.421+633C>G
NM_000296.3:c.3460C>G	NP_000287.3:p.Pro1154Ala
NM_001009944.2:c.3460C>G	NP_001009944.2:p.Pro1154Ala
XM_005255370.2:c.415C>G	XP_005255427.1:p.Pro139Ala
XM_011522525.1:c.3538C>G	XP_011520827.1:p.Pro1180Ala
XM_011522526.1:c.3538C>G	XP_011520828.1:p.Pro1180Ala
XM_011522527.1:c.3538C>G	XP_011520829.1:p.Pro1180Ala
XM_011522528.1:c.3514C>G	XP_011520830.1:p.Pro1172Ala
XM_011522529.1:c.3514C>G	XP_011520831.1:p.Pro1172Ala
XM_011522530.1:c.3484C>G	XP_011520832.1:p.Pro1162Ala
XM_011522531.1:c.3466C>G	XP_011520833.1:p.Pro1156Ala
XM_011522532.1:c.3412C>G	XP_011520834.1:p.Pro1138Ala
XM_011522533.1:c.3331C>G	XP_011520835.1:p.Pro1111Ala
XM_011522534.1:c.3274C>G	XP_011520836.1:p.Pro1092Ala
XM_011522535.1:c.1360C>G	XP_011520837.1:p.Pro454Ala
XM_011522536.1:c.3538C>G	XP_011520838.1:p.Pro1180Ala
XM_011522537.1:c.538C>G	XP_011520839.1:p.Pro180Ala
XR_932867.1:n.3553C>G
XR_932868.1:n.3553C>G
XR_932869.1:n.3553C>G
XR_932870.1:n.3553C>G
XM_005255370.3:c.415C>G	XP_005255427.1:p.Pro139Ala
XM_011522528.3:c.3514C>G	XP_011520830.1:p.Pro1172Ala
XM_011522529.2:c.3514C>G	XP_011520831.1:p.Pro1172Ala
XM_011522537.2:c.538C>G	XP_011520839.1:p.Pro180Ala
XM_024450298.1:c.3580C>G	XP_024306066.1:p.Pro1194Ala
XM_024450299.1:c.3508C>G	XP_024306067.1:p.Pro1170Ala
XM_024450300.1:c.3370C>G	XP_024306068.1:p.Pro1124Ala
XM_024450301.1:c.1456C>G	XP_024306069.1:p.Pro486Ala
NM_000296.4:c.3460C>G	NP_000287.4:p.Pro1154Ala
NM_001009944.3:c.3460C>G MANE Select	NP_001009944.3:p.Pro1154Ala