Canonical Allele Identifier: CA961019600

Gene: MMP14

Linked Data

• dbSNP Id: rs2039784987
• gnomAD v3: 14-22843089-GGCTTTGT-G
• gnomAD v4: 14-22843089-GGCTTTGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22843094_22843100del , CM000676.2:g.22843094_22843100del	GRCh38
NC_000014.8:g.23312303_23312309del , CM000676.1:g.23312303_23312309del	GRCh37
NC_000014.7:g.22382143_22382149del	NCBI36
NG_046989.1:g.11562_11568del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311852.11:c.689-163_689-157del MANE Select	ENSP00000308208.6:n.689-163_689-157del
ENST00000548162.2:c.689-163_689-157del	ENSP00000506068.1:n.689-163_689-157del
ENST00000680097.1:c.*4-163_*4-157del	ENSP00000506631.1:n.*4-163_*4-157del
ENST00000680941.1:c.*8_*14del	ENSP00000506378.1:n.*8_*14del
ENST00000311852.10:c.689-163_689-157del	ENSP00000308208.6:n.689-163_689-157del
ENST00000548162.1:n.931-163_931-157del
NM_004995.3:c.689-163_689-157del	NP_004986.1:n.689-163_689-157del
NM_004995.4:c.689-163_689-157del MANE Select	NP_004986.1:n.689-163_689-157del