Canonical Allele Identifier: CA2816196995

Gene: RALY

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34000323T>C , CM000682.2:g.34000323T>C	GRCh38
NC_000020.10:g.32588129T>C , CM000682.1:g.32588129T>C	GRCh37
NC_000020.9:g.32051790T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246194.8:c.-93+6192T>C MANE Select	ENSP00000246194.3:n.-93+6192T>C
ENST00000246194.7:c.-93+6192T>C	ENSP00000246194.3:n.-93+6192T>C
ENST00000333552.9:c.-93+6192T>C	ENSP00000327522.5:n.-93+6192T>C
ENST00000375114.7:c.-93+6192T>C	ENSP00000364255.3:n.-93+6192T>C
ENST00000413297.5:c.-169+6192T>C	ENSP00000403744.1:n.-169+6192T>C
ENST00000448364.5:c.-210+6192T>C	ENSP00000413638.1:n.-210+6192T>C
NM_007367.3:c.-93+6192T>C	NP_031393.2:n.-93+6192T>C
NM_016732.2:c.-93+6192T>C	NP_057951.1:n.-93+6192T>C
XM_005260334.3:c.-10+6192T>C	XP_005260391.1:n.-10+6192T>C
XM_005260336.3:c.-10+6192T>C	XP_005260393.1:n.-10+6192T>C
XM_011528695.1:c.-210+6192T>C	XP_011526997.1:n.-210+6192T>C
XM_005260334.5:c.-10+6192T>C	XP_005260391.1:n.-10+6192T>C
XM_005260336.5:c.-10+6192T>C	XP_005260393.1:n.-10+6192T>C
XM_011528695.3:c.-210+6192T>C	XP_011526997.1:n.-210+6192T>C
XM_017027731.2:c.-10+6192T>C	XP_016883220.1:n.-10+6192T>C
XM_024451859.1:c.-93+6192T>C	XP_024307627.1:n.-93+6192T>C
NM_016732.3:c.-93+6192T>C MANE Select	NP_057951.1:n.-93+6192T>C
NM_007367.4:c.-93+6192T>C	NP_031393.2:n.-93+6192T>C