Canonical Allele Identifier: CA2655998056

Gene: RASL10A

Linked Data

• gnomAD v4: 22-29313076-CCCAGAAAGGACTGGTCATCTCCAATGGAGCTTGGGACCTGGTTGGGTCCAATGAGGTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29313078_29313135del , CM000684.2:g.29313078_29313135del	GRCh38
NC_000022.10:g.29709067_29709124del , CM000684.1:g.29709067_29709124del	GRCh37
NC_000022.9:g.28039067_28039124del	NCBI36
NG_032959.1:g.11072_11129del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216101.7:c.*167_*224del MANE Select	ENSP00000216101.6:n.*167_*224del
ENST00000216101.6:c.*167_*224del	ENSP00000216101.6:n.*167_*224del
ENST00000401450.3:c.*725_*782del	ENSP00000386095.3:n.*725_*782del
NM_006477.4:c.*167_*224del	NP_006468.1:n.*167_*224del
XM_011529821.1:c.*167_*224del	XP_011528123.1:n.*167_*224del
XM_011529822.1:c.*167_*224del	XP_011528124.1:n.*167_*224del
XM_011529823.1:c.*167_*224del	XP_011528125.1:n.*167_*224del
NM_006477.5:c.*167_*224del MANE Select	NP_006468.1:n.*167_*224del