Canonical Allele Identifier: CA12499753
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs12670798

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21567734T>C , CM000669.2:g.21567734T>C GRCh38
NC_000007.13:g.21607352T>C , CM000669.1:g.21607352T>C GRCh37
NC_000007.12:g.21573877T>C NCBI36
NG_012886.2:g.29520T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.1195-2335T>C MANE Select ENSP00000475939.1:n.1195-2335T>C
ENST00000328843.10:c.1195-2335T>C ENSP00000330671.7:n.1195-2335T>C
ENST00000409508.7:c.1195-2335T>C ENSP00000475939.1:n.1195-2335T>C
ENST00000496218.1:n.81-2335T>C
ENST00000620169.4:c.1195-2335T>C ENSP00000481693.1:n.1195-2335T>C
NM_001277115.1:c.1195-2335T>C NP_001264044.1:n.1195-2335T>C
XR_927090.1:n.563+5592A>G
XR_001745114.1:n.2793+5592A>G
NM_001277115.2:c.1195-2335T>C MANE Select NP_001264044.1:n.1195-2335T>C