Canonical Allele Identifier: CA1744291

Gene: GNLY

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85695345T>C , CM000664.2:g.85695345T>C	GRCh38
NC_000002.11:g.85922468T>C , CM000664.1:g.85922468T>C	GRCh37
NC_000002.10:g.85775979T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006433.5:c.78T>C MANE Select	NP_006424.2:p.Pro26=
ENST00000263863.9:c.78T>C MANE Select	ENSP00000263863.5:p.Pro26=
NM_001302758.1:c.159T>C	NP_001289687.1:p.Pro53=
NM_001302758.2:c.159T>C	NP_001289687.1:p.Pro53=
NM_006433.4:c.78T>C	NP_006424.2:p.Pro26=
NM_012483.3:c.33T>C	NP_036615.2:p.Pro11=
NM_012483.4:c.33T>C	NP_036615.2:p.Pro11=
ENST00000263863.8:c.78T>C	ENSP00000263863.4:p.Pro26=
ENST00000409696.7:c.33T>C	ENSP00000387116.3:p.Pro11=
ENST00000464298.5:n.340T>C
ENST00000470974.1:n.732T>C
ENST00000482900.5:n.195T>C
ENST00000488945.5:n.73T>C
ENST00000489214.5:n.448T>C
ENST00000489980.5:n.1004T>C
ENST00000491234.1:n.309T>C
ENST00000524600.5:c.159T>C	ENSP00000436423.1:p.Pro53=
ENST00000531685.1:n.209T>C
ENST00000533041.5:n.361T>C
ENST00000534351.5:n.242T>C
XM_005264084.2:c.159T>C	XP_005264141.1:p.Pro53=
XM_005264085.2:c.78T>C	XP_005264142.1:p.Pro26=
XM_005264087.2:c.33T>C	XP_005264144.1:p.Pro11=
XM_011532480.1:c.159T>C	XP_011530782.1:p.Pro53=
XM_011532481.1:c.159T>C	XP_011530783.1:p.Pro53=