Canonical Allele Identifier: CA806248957

Gene: ADAM19

Linked Data

• dbSNP Id: rs1183946877
• gnomAD v3: 5-157543127-T-TAC
• gnomAD v4: 5-157543127-T-TAC
• MyVariant Identifiers: chr5:g.156970135_156970136insAC (hg19) ; chr5:g.157543127_157543128insAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157543136_157543137dup , CM000667.2:g.157543136_157543137dup	GRCh38
NC_000005.9:g.156970144_156970145dup , CM000667.1:g.156970144_156970145dup	GRCh37
NC_000005.8:g.156902722_156902723dup	NCBI36
NG_046960.1:g.37695_37696dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000257527.9:c.252-5138_252-5137dup MANE Select	ENSP00000257527.5:n.252-5138_252-5137dup
ENST00000257527.8:c.252-5138_252-5137dup	ENSP00000257527.4:n.252-5138_252-5137dup
ENST00000517905.1:c.252-5138_252-5137dup	ENSP00000428654.1:n.252-5138_252-5137dup
ENST00000517951.5:c.252-5138_252-5137dup	ENSP00000428376.1:n.252-5138_252-5137dup
NM_033274.4:c.252-5138_252-5137dup	NP_150377.1:n.252-5138_252-5137dup
XM_005266003.2:c.252-5138_252-5137dup	XP_005266060.1:n.252-5138_252-5137dup
NM_033274.5:c.252-5138_252-5137dup MANE Select	NP_150377.1:n.252-5138_252-5137dup