Canonical Allele Identifier: CA1956120889
Gene: NAV2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19548404_19548407delinsACCT , CM000673.2:g.19548404_19548407delinsACCT GRCh38
NC_000011.9:g.19569951_19569954delinsACCT , CM000673.1:g.19569951_19569954delinsACCT GRCh37
NC_000011.8:g.19526527_19526530delinsACCT NCBI36
NG_030347.1:g.202681_202684delinsACCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360655.8:c.75+197377_75+197380delinsACCT ENSP00000353871.4:n.75+197377_75+197380delinsACCT
NM_001111018.1:c.75+197377_75+197380delinsACCT NP_001104488.1:n.75+197377_75+197380delinsACCT
XM_011520452.1:c.75+197377_75+197380delinsACCT XP_011518754.1:n.75+197377_75+197380delinsACCT
XM_011520452.2:c.75+197377_75+197380delinsACCT XP_011518754.1:n.75+197377_75+197380delinsACCT
XM_017018520.2:c.75+197377_75+197380delinsACCT XP_016874009.1:n.75+197377_75+197380delinsACCT
XM_017018522.1:c.75+197377_75+197380delinsACCT XP_016874011.1:n.75+197377_75+197380delinsACCT
XM_024448758.1:c.75+197377_75+197380delinsACCT XP_024304526.1:n.75+197377_75+197380delinsACCT
NM_001111018.2:c.75+197377_75+197380delinsACCT NP_001104488.1:n.75+197377_75+197380delinsACCT