Canonical Allele Identifier: CA323103345

Gene: RASL10A

Linked Data

• dbSNP Id: rs1048962
• MyVariant Identifiers: chr22:g.29709096T>A (hg19) ; chr22:g.29313107T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29313107T>A , CM000684.2:g.29313107T>A	GRCh38
NC_000022.10:g.29709096T>A , CM000684.1:g.29709096T>A	GRCh37
NC_000022.9:g.28039096T>A	NCBI36
NG_032959.1:g.11101T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000216101.7:c.*194A>T MANE Select	ENSP00000216101.6:n.*194A>T
ENST00000216101.6:c.*194A>T	ENSP00000216101.6:n.*194A>T
ENST00000401450.3:c.*752A>T	ENSP00000386095.3:n.*752A>T
NM_006477.4:c.*194A>T	NP_006468.1:n.*194A>T
XM_011529821.1:c.*194A>T	XP_011528123.1:n.*194A>T
XM_011529822.1:c.*194A>T	XP_011528124.1:n.*194A>T
XM_011529823.1:c.*194A>T	XP_011528125.1:n.*194A>T
NM_006477.5:c.*194A>T MANE Select	NP_006468.1:n.*194A>T