Canonical Allele Identifier: CA359206042

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13717436C>A (hg19) ; chr5:g.13717327C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717327C>A , CM000667.2:g.13717327C>A	GRCh38
NC_000005.9:g.13717436C>A , CM000667.1:g.13717436C>A	GRCh37
NC_000005.8:g.13770436C>A	NCBI36
NG_013081.1:g.232154G>T
NG_013081.2:g.232154G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.12693G>T MANE Select	ENSP00000265104.4:p.Met4231Ile
ENST00000681290.1:c.12648G>T	ENSP00000505288.1:p.Met4216Ile
ENST00000265104.4:c.12693G>T	ENSP00000265104.4:p.Met4231Ile
NM_001369.2:c.12693G>T	NP_001360.1:p.Met4231Ile
XM_005248262.2:c.12648G>T	XP_005248319.1:p.Met4216Ile
XM_005248262.3:c.12801G>T	XP_005248319.2:p.Met4267Ile
XM_017009177.1:c.12801G>T	XP_016864666.1:p.Met4267Ile
XM_017009178.1:c.11706G>T	XP_016864667.1:p.Met3902Ile
XM_017009179.2:c.11706G>T	XP_016864668.1:p.Met3902Ile
XM_017009180.1:c.12801G>T	XP_016864669.1:p.Met4267Ile
XM_017009185.1:c.7890G>T	XP_016864674.1:p.Met2630Ile
XM_017009186.1:c.7443G>T	XP_016864675.1:p.Met2481Ile
XM_017009188.1:c.6780G>T	XP_016864677.1:p.Met2260Ile
XM_024454388.1:c.11706G>T	XP_024310156.1:p.Met3902Ile
XM_024454389.1:c.11295G>T	XP_024310157.1:p.Met3765Ile
NM_001369.3:c.12693G>T MANE Select	NP_001360.1:p.Met4231Ile