Canonical Allele Identifier: CA359207928
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13776459G>A , CM000667.2:g.13776459G>A GRCh38
NC_000005.9:g.13776568G>A , CM000667.1:g.13776568G>A GRCh37
NC_000005.8:g.13829568G>A NCBI36
NG_013081.1:g.173022C>T
NG_013081.2:g.173022C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9353C>T MANE Select ENSP00000265104.4:p.Pro3118Leu
ENST00000681290.1:c.9308C>T ENSP00000505288.1:p.Pro3103Leu
ENST00000265104.4:c.9353C>T ENSP00000265104.4:p.Pro3118Leu
NM_001369.2:c.9353C>T NP_001360.1:p.Pro3118Leu
XM_005248262.2:c.9308C>T XP_005248319.1:p.Pro3103Leu
XM_005248262.3:c.9461C>T XP_005248319.2:p.Pro3154Leu
XM_017009177.1:c.9461C>T XP_016864666.1:p.Pro3154Leu
XM_017009178.1:c.8366C>T XP_016864667.1:p.Pro2789Leu
XM_017009179.2:c.8366C>T XP_016864668.1:p.Pro2789Leu
XM_017009180.1:c.9461C>T XP_016864669.1:p.Pro3154Leu
XM_017009181.1:c.9461C>T XP_016864670.1:p.Pro3154Leu
XM_017009182.1:c.9461C>T XP_016864671.1:p.Pro3154Leu
XM_017009183.1:c.9461C>T XP_016864672.1:p.Pro3154Leu
XM_017009185.1:c.4550C>T XP_016864674.1:p.Pro1517Leu
XM_017009186.1:c.4103C>T XP_016864675.1:p.Pro1368Leu
XM_017009188.1:c.3440C>T XP_016864677.1:p.Pro1147Leu
XM_024454388.1:c.8366C>T XP_024310156.1:p.Pro2789Leu
XM_024454389.1:c.7955C>T XP_024310157.1:p.Pro2652Leu
NM_001369.3:c.9353C>T MANE Select NP_001360.1:p.Pro3118Leu