Canonical Allele Identifier: CA359208581

Gene: DNAH5

Linked Data

• COSMIC: COSM6101858
• MyVariant Identifiers: chr5:g.13776646C>G (hg19) ; chr5:g.13776537C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776537C>G , CM000667.2:g.13776537C>G	GRCh38
NC_000005.9:g.13776646C>G , CM000667.1:g.13776646C>G	GRCh37
NC_000005.8:g.13829646C>G	NCBI36
NG_013081.1:g.172944G>C
NG_013081.2:g.172944G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9275G>C MANE Select	ENSP00000265104.4:p.Gly3092Ala
ENST00000681290.1:c.9230G>C	ENSP00000505288.1:p.Gly3077Ala
ENST00000265104.4:c.9275G>C	ENSP00000265104.4:p.Gly3092Ala
NM_001369.2:c.9275G>C	NP_001360.1:p.Gly3092Ala
XM_005248262.2:c.9230G>C	XP_005248319.1:p.Gly3077Ala
XM_005248262.3:c.9383G>C	XP_005248319.2:p.Gly3128Ala
XM_017009177.1:c.9383G>C	XP_016864666.1:p.Gly3128Ala
XM_017009178.1:c.8288G>C	XP_016864667.1:p.Gly2763Ala
XM_017009179.2:c.8288G>C	XP_016864668.1:p.Gly2763Ala
XM_017009180.1:c.9383G>C	XP_016864669.1:p.Gly3128Ala
XM_017009181.1:c.9383G>C	XP_016864670.1:p.Gly3128Ala
XM_017009182.1:c.9383G>C	XP_016864671.1:p.Gly3128Ala
XM_017009183.1:c.9383G>C	XP_016864672.1:p.Gly3128Ala
XM_017009185.1:c.4472G>C	XP_016864674.1:p.Gly1491Ala
XM_017009186.1:c.4025G>C	XP_016864675.1:p.Gly1342Ala
XM_017009188.1:c.3362G>C	XP_016864677.1:p.Gly1121Ala
XM_024454388.1:c.8288G>C	XP_024310156.1:p.Gly2763Ala
XM_024454389.1:c.7877G>C	XP_024310157.1:p.Gly2626Ala
NM_001369.3:c.9275G>C MANE Select	NP_001360.1:p.Gly3092Ala