Canonical Allele Identifier: CA1697922611

Gene: AQP1

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30924207G>A , CM000669.2:g.30924207G>A	GRCh38
NC_000007.13:g.30963822G>A , CM000669.1:g.30963822G>A	GRCh37
NC_000007.12:g.30930347G>A	NCBI36
NG_007475.2:g.75814G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311813.11:c.*578G>A MANE Select	ENSP00000311165.4:n.*578G>A
ENST00000441328.7:n.522G>A
ENST00000652692.1:c.622+554G>A
ENST00000652696.1:c.*405G>A	ENSP00000498672.1:n.*405G>A
ENST00000311813.8:c.*578G>A	ENSP00000311165.4:n.*578G>A
ENST00000441328.6:c.*578G>A	ENSP00000405698.2:n.*578G>A
NM_001185060.1:c.*578G>A	NP_001171989.1:n.*578G>A
NM_001185061.1:c.*578G>A	NP_001171990.1:n.*578G>A
NM_001185062.1:c.*578G>A	NP_001171991.1:n.*578G>A
NM_198098.2:c.*578G>A	NP_932766.1:n.*578G>A
NM_001329872.1:c.*198G>A	NP_001316801.1:n.*198G>A
NM_198098.3:c.*578G>A	NP_932766.1:n.*578G>A
NM_001329872.2:c.*198G>A	NP_001316801.1:n.*198G>A
NM_198098.4:c.*578G>A MANE Select	NP_932766.1:n.*578G>A