Canonical Allele Identifier: CA381939540

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76925734G>C (hg19) ; chr11:g.77214689G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214689G>C , CM000673.2:g.77214689G>C	GRCh38
NC_000011.9:g.76925734G>C , CM000673.1:g.76925734G>C	GRCh37
NC_000011.8:g.76603382G>C	NCBI36
NG_009086.1:g.91425G>C
NG_009086.2:g.91444G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6641G>C MANE Select	ENSP00000386331.3:p.Gly2214Ala
ENST00000670577.1:c.4442G>C
ENST00000409619.6:c.6494G>C	ENSP00000386635.2:p.Gly2165Ala
ENST00000409709.7:c.6641G>C	ENSP00000386331.3:p.Gly2214Ala
ENST00000458169.2:c.4067G>C	ENSP00000417017.2:p.Gly1356Ala
ENST00000458637.6:c.6521G>C	ENSP00000392185.2:p.Gly2174Ala
ENST00000481328.7:n.5191G>C
ENST00000605744.1:n.2155G>C
NM_000260.3:c.6641G>C	NP_000251.3:p.Gly2214Ala
NM_001127180.1:c.6521G>C	NP_001120652.1:p.Gly2174Ala
XM_005274012.2:c.6524G>C	XP_005274069.1:p.Gly2175Ala
XM_006718561.2:c.6527G>C	XP_006718624.1:p.Gly2176Ala
XR_949941.1:n.6935G>C
XM_017017780.1:c.6731G>C	XP_016873269.1:p.Gly2244Ala
XM_017017784.1:c.6614G>C	XP_016873273.1:p.Gly2205Ala
XM_017017788.1:c.6617G>C	XP_016873277.1:p.Gly2206Ala
XR_001747885.1:n.6720G>C
XR_001747887.1:n.6706G>C
NM_000260.4:c.6641G>C MANE Select	NP_000251.3:p.Gly2214Ala
NM_001127180.2:c.6521G>C	NP_001120652.1:p.Gly2174Ala
NM_001369365.1:c.6494G>C	NP_001356294.1:p.Gly2165Ala