Canonical Allele Identifier: CA2259200814

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665912_39665915delinsAAGG , CM000679.2:g.39665912_39665915delinsAAGG	GRCh38
NC_000017.10:g.37822165_37822168delinsAAGG , CM000679.1:g.37822165_37822168delinsAAGG	GRCh37
NC_000017.9:g.35075691_35075694delinsAAGG	NCBI36
NG_008892.1:g.5567_5570delinsAAGG , LRG_210:g.5567_5570delinsAAGG
NG_042278.1:g.2932_2935delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.307_310delinsAAGG MANE Select	ENSP00000312624.2:p.Lys103=
ENST00000309889.2:c.307_310delinsAAGG	ENSP00000312624.2:p.Lys103=
ENST00000578283.1:c.235_238delinsAAGG	ENSP00000462787.1:p.Lys79=
NM_003673.3:c.307_310delinsAAGG , LRG_210t1:c.307_310delinsAAGG	NP_003664.1:p.Lys103=
NM_003673.4:c.307_310delinsAAGG MANE Select	NP_003664.1:p.Lys103=