Canonical Allele Identifier: CA1528395742

Gene: DNAH5

Linked Data

• dbSNP Id: rs1740720586
• gnomAD v4: 5-13691772-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13691772T>G , CM000667.2:g.13691772T>G	GRCh38
NC_000005.9:g.13691881T>G , CM000667.1:g.13691881T>G	GRCh37
NC_000005.8:g.13744881T>G	NCBI36
NG_013081.1:g.257709A>C
NG_013081.2:g.257709A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1420A>C
ENST00000265104.5:c.*212A>C MANE Select	ENSP00000265104.4:n.*212A>C
ENST00000681290.1:c.*212A>C	ENSP00000505288.1:n.*212A>C
ENST00000265104.4:c.*212A>C	ENSP00000265104.4:n.*212A>C
NM_001369.2:c.*212A>C	NP_001360.1:n.*212A>C
XM_005248262.2:c.*212A>C	XP_005248319.1:n.*212A>C
XM_005248262.3:c.*212A>C	XP_005248319.2:n.*212A>C
XM_017009177.1:c.*212A>C	XP_016864666.1:n.*212A>C
XM_017009178.1:c.*212A>C	XP_016864667.1:n.*212A>C
XM_017009179.2:c.*212A>C	XP_016864668.1:n.*212A>C
XM_017009185.1:c.*212A>C	XP_016864674.1:n.*212A>C
XM_017009186.1:c.*212A>C	XP_016864675.1:n.*212A>C
XM_017009188.1:c.*212A>C	XP_016864677.1:n.*212A>C
XM_024454388.1:c.*212A>C	XP_024310156.1:n.*212A>C
XM_024454389.1:c.*212A>C	XP_024310157.1:n.*212A>C
NM_001369.3:c.*212A>C MANE Select	NP_001360.1:n.*212A>C