Canonical Allele Identifier: CA1240109503
Gene: EMILIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27084848_27084849delinsTA , CM000664.2:g.27084848_27084849delinsTA GRCh38
NC_000002.11:g.27307716_27307717delinsTA , CM000664.1:g.27307716_27307717delinsTA GRCh37
NC_000002.10:g.27161220_27161221delinsTA NCBI36
NG_012199.1:g.3106_3107delinsTA
NG_046849.1:g.11282_11283delinsTA
NG_012199.2:g.3106_3107delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000380320.9:c.2558-143_2558-142delinsTA MANE Select ENSP00000369677.4:n.2558-143_2558-142deli...
ENST00000380320.8:c.2558-143_2558-142delinsTA ENSP00000369677.4:n.2558-143_2558-142deli...
ENST00000433140.1:c.550-143_550-142delinsTA
NM_007046.3:c.2558-143_2558-142delinsTA NP_008977.1:n.2558-143_2558-142delinsTA
XM_006711928.2:c.2558-143_2558-142delinsTA XP_006711991.1:n.2558-143_2558-142delinsT...
NM_007046.4:c.2558-143_2558-142delinsTA MANE Select NP_008977.1:n.2558-143_2558-142delinsTA