Canonical Allele Identifier: CA1340096606

Gene: CHL1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.212236_212237delinsAT , CM000665.2:g.212236_212237delinsAT	GRCh38
NC_000003.11:g.253919_253920delinsAT , CM000665.1:g.253919_253920delinsAT	GRCh37
NC_000003.10:g.228919_228920delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000256509.7:c.-175+15173_-175+15174delinsAT MANE Select	ENSP00000256509.2:n.-175+15173_-175+15174delinsAT
ENST00000256509.6:c.-175+15173_-175+15174delinsAT	ENSP00000256509.2:n.-175+15173_-175+15174delinsAT
ENST00000397491.6:c.-175+15173_-175+15174delinsAT	ENSP00000380628.2:n.-175+15173_-175+15174delinsAT
ENST00000421198.5:c.-175+14868_-175+14869delinsAT	ENSP00000413628.1:n.-175+14868_-175+14869delinsAT
ENST00000427688.5:c.-95+15173_-95+15174delinsAT	ENSP00000403311.1:n.-95+15173_-95+15174delinsAT
ENST00000435603.5:c.-95+14144_-95+14145delinsAT	ENSP00000397445.1:n.-95+14144_-95+14145delinsAT
ENST00000453040.5:c.*164+14144_*164+14145delinsAT	ENSP00000413109.1:n.*164+14144_*164+14145delinsAT
ENST00000481167.5:n.293+15173_293+15174delinsAT
ENST00000486881.1:n.80-968_80-967delinsAT
ENST00000489224.5:n.450+14144_450+14145delinsAT
NM_001253387.1:c.-175+15173_-175+15174delinsAT	NP_001240316.1:n.-175+15173_-175+15174delinsAT
NM_006614.3:c.-175+15173_-175+15174delinsAT	NP_006605.2:n.-175+15173_-175+15174delinsAT
NR_045572.1:n.450+14144_450+14145delinsAT
XM_006712938.1:c.-175+14868_-175+14869delinsAT	XP_006713001.1:n.-175+14868_-175+14869delinsAT
XM_006712939.2:c.-95+15173_-95+15174delinsAT	XP_006713002.1:n.-95+15173_-95+15174delinsAT
XM_006712940.2:c.-95+14144_-95+14145delinsAT	XP_006713003.1:n.-95+14144_-95+14145delinsAT
XM_011533292.1:c.-175+14144_-175+14145delinsAT	XP_011531594.1:n.-175+14144_-175+14145delinsAT
XM_011533294.1:c.-175+14868_-175+14869delinsAT	XP_011531596.1:n.-175+14868_-175+14869delinsAT
XM_011533295.1:c.-175+14144_-175+14145delinsAT	XP_011531597.1:n.-175+14144_-175+14145delinsAT
XM_011533296.1:c.-175+14868_-175+14869delinsAT	XP_011531598.1:n.-175+14868_-175+14869delinsAT
XM_011533297.1:c.-175+14868_-175+14869delinsAT	XP_011531599.1:n.-175+14868_-175+14869delinsAT
XM_006712939.3:c.-95+15173_-95+15174delinsAT	XP_006713002.1:n.-95+15173_-95+15174delinsAT
XM_006712940.3:c.-95+14144_-95+14145delinsAT	XP_006713003.1:n.-95+14144_-95+14145delinsAT
XM_017005566.1:c.-4671-968_-4671-967delinsAT	XP_016861055.1:n.-4671-968_-4671-967delinsAT
XM_017005567.1:c.-95+14868_-95+14869delinsAT	XP_016861056.1:n.-95+14868_-95+14869delinsAT
XM_017005569.1:c.-95+15173_-95+15174delinsAT	XP_016861058.1:n.-95+15173_-95+15174delinsAT
XM_017005570.1:c.-95+14144_-95+14145delinsAT	XP_016861059.1:n.-95+14144_-95+14145delinsAT
XM_017005571.1:c.-95+14868_-95+14869delinsAT	XP_016861060.1:n.-95+14868_-95+14869delinsAT
XM_017005572.1:c.-175+15173_-175+15174delinsAT	XP_016861061.1:n.-175+15173_-175+15174delinsAT
XM_017005573.1:c.-95+15173_-95+15174delinsAT	XP_016861062.1:n.-95+15173_-95+15174delinsAT
NM_006614.4:c.-175+15173_-175+15174delinsAT MANE Select	NP_006605.2:n.-175+15173_-175+15174delinsAT
NR_045572.2:n.204+14144_204+14145delinsAT
NM_001253387.2:c.-175+15173_-175+15174delinsAT	NP_001240316.1:n.-175+15173_-175+15174delinsAT