Canonical Allele Identifier: CA359191900

Gene: DNAH5

Linked Data

• dbSNP Id: rs1454812319
• MyVariant Identifiers: chr5:g.13753545A>G (hg19) ; chr5:g.13753436A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753436A>G , CM000667.2:g.13753436A>G	GRCh38
NC_000005.9:g.13753545A>G , CM000667.1:g.13753545A>G	GRCh37
NC_000005.8:g.13806545A>G	NCBI36
NG_013081.1:g.196045T>C
NG_013081.2:g.196045T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10669T>C MANE Select	ENSP00000265104.4:p.Phe3557Leu
ENST00000681290.1:c.10624T>C	ENSP00000505288.1:p.Phe3542Leu
ENST00000265104.4:c.10669T>C	ENSP00000265104.4:p.Phe3557Leu
NM_001369.2:c.10669T>C	NP_001360.1:p.Phe3557Leu
XM_005248262.2:c.10624T>C	XP_005248319.1:p.Phe3542Leu
XM_005248262.3:c.10777T>C	XP_005248319.2:p.Phe3593Leu
XM_017009177.1:c.10777T>C	XP_016864666.1:p.Phe3593Leu
XM_017009178.1:c.9682T>C	XP_016864667.1:p.Phe3228Leu
XM_017009179.2:c.9682T>C	XP_016864668.1:p.Phe3228Leu
XM_017009180.1:c.10777T>C	XP_016864669.1:p.Phe3593Leu
XM_017009181.1:c.10777T>C	XP_016864670.1:p.Phe3593Leu
XM_017009182.1:c.10777T>C	XP_016864671.1:p.Phe3593Leu
XM_017009185.1:c.5866T>C	XP_016864674.1:p.Phe1956Leu
XM_017009186.1:c.5419T>C	XP_016864675.1:p.Phe1807Leu
XM_017009188.1:c.4756T>C	XP_016864677.1:p.Phe1586Leu
XM_024454388.1:c.9682T>C	XP_024310156.1:p.Phe3228Leu
XM_024454389.1:c.9271T>C	XP_024310157.1:p.Phe3091Leu
NM_001369.3:c.10669T>C MANE Select	NP_001360.1:p.Phe3557Leu