Canonical Allele Identifier: CA2466480464

Gene: SSR4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153797952_153797957delinsTCTCTC , CM000685.2:g.153797952_153797957delinsTCTCTC	GRCh38
NC_000023.10:g.153063407_153063412delinsTCTCTC , CM000685.1:g.153063407_153063412delinsTCTCTC	GRCh37
NC_000023.9:g.152716601_152716606delinsTCTCTC	NCBI36
NG_041795.1:g.8778_8783delinsTCTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370086.8:c.352-119_352-114delinsTCTCTC MANE Select	ENSP00000359103.3:n.352-119_352-114delinsTCTCTC
ENST00000320857.7:c.352-119_352-114delinsTCTCTC	ENSP00000317331.3:n.352-119_352-114delinsTCTCTC
ENST00000370085.3:c.277-119_277-114delinsTCTCTC	ENSP00000359102.3:n.277-119_277-114delinsTCTCTC
ENST00000370086.7:c.352-119_352-114delinsTCTCTC	ENSP00000359103.3:n.352-119_352-114delinsTCTCTC
ENST00000370087.5:c.352-119_352-114delinsTCTCTC	ENSP00000359104.1:n.352-119_352-114delinsTCTCTC
ENST00000447375.1:n.192-119_192-114delinsTCTCTC
ENST00000460616.5:n.2060-119_2060-114delinsTCTCTC
ENST00000471880.5:n.555-119_555-114delinsTCTCTC
ENST00000482902.5:n.2179-119_2179-114delinsTCTCTC
ENST00000485612.5:n.467-119_467-114delinsTCTCTC
ENST00000486204.5:n.424-119_424-114delinsTCTCTC
NM_001204526.1:c.385-119_385-114delinsTCTCTC	NP_001191455.1:n.385-119_385-114delinsTCTCTC
NM_001204527.1:c.376-119_376-114delinsTCTCTC	NP_001191456.1:n.376-119_376-114delinsTCTCTC
NM_006280.2:c.352-119_352-114delinsTCTCTC	NP_006271.1:n.352-119_352-114delinsTCTCTC
NR_037927.1:n.697-119_697-114delinsTCTCTC
XM_011531186.1:c.352-119_352-114delinsTCTCTC	XP_011529488.1:n.352-119_352-114delinsTCTCTC
XM_011531187.1:c.352-119_352-114delinsTCTCTC	XP_011529489.1:n.352-119_352-114delinsTCTCTC
XM_017029756.1:c.163-119_163-114delinsTCTCTC	XP_016885245.1:n.163-119_163-114delinsTCTCTC
XM_017029757.1:c.163-119_163-114delinsTCTCTC	XP_016885246.1:n.163-119_163-114delinsTCTCTC
XM_024452428.1:c.163-119_163-114delinsTCTCTC	XP_024308196.1:n.163-119_163-114delinsTCTCTC
NM_001204527.2:c.376-119_376-114delinsTCTCTC	NP_001191456.1:n.376-119_376-114delinsTCTCTC
NM_006280.3:c.352-119_352-114delinsTCTCTC MANE Select	NP_006271.1:n.352-119_352-114delinsTCTCTC